-
1
-
-
0029877887
-
The effect of Y-chromosome alpha-satellite length on the rate of sex chromosome disomy in human sperm
-
Abruzzo MA, Griffin DK, Millie EA, Sheean LA, Hassold TJ (1996) The effect of Y-chromosome alpha-satellite length on the rate of sex chromosome disomy in human sperm. Hum Genet 97 : 819-823
-
(1996)
Hum Genet
, vol.97
, pp. 819-823
-
-
Abruzzo, M.A.1
Griffin, D.K.2
Millie, E.A.3
Sheean, L.A.4
Hassold, T.J.5
-
2
-
-
0027462062
-
Human chromosome 21: Genome mapping and exploration, circa 1993
-
Antonarakis SE (1993) Human chromosome 21: genome mapping and exploration, circa 1993. Trends Genet 9 : 142-148
-
(1993)
Trends Genet
, vol.9
, pp. 142-148
-
-
Antonarakis, S.E.1
-
3
-
-
0023853503
-
G-band position on meiotic synapsis and crossing over
-
Ashley T (1988) G-band position on meiotic synapsis and crossing over. Genetics 118 : 307-317
-
(1988)
Genetics
, vol.118
, pp. 307-317
-
-
Ashley, T.1
-
4
-
-
0021039877
-
Segregation of chromosomes into the spermatozoa of a man heterozygous for a 14;21 Robertsonian translocation
-
Balkan W, Martin RH (1983a) Segregation of chromosomes into the spermatozoa of a man heterozygous for a 14;21 Robertsonian translocation. Am J Med Genet 16 : 169-172
-
(1983)
Am J Med Genet
, vol.16
, pp. 169-172
-
-
Balkan, W.1
Martin, R.H.2
-
5
-
-
0020560397
-
Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations
-
Balkan W, Martin RH (1983b) Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations. Hum Genet 63 : 345-348
-
(1983)
Hum Genet
, vol.63
, pp. 345-348
-
-
Balkan, W.1
Martin, R.H.2
-
6
-
-
0020955265
-
Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 3
-
Balkan W, Burns K, Martin RH (1983) Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 3. Cytogenet Cell Genet 35 : 295-297
-
(1983)
Cytogenet Cell Genet
, vol.35
, pp. 295-297
-
-
Balkan, W.1
Burns, K.2
Martin, R.H.3
-
7
-
-
0023944147
-
Sperm chromosome complements in a 47,XYY man
-
Benet J, Martin RH (1988) Sperm chromosome complements in a 47,XYY man. Hum Genet 78 : 313-315
-
(1988)
Hum Genet
, vol.78
, pp. 313-315
-
-
Benet, J.1
Martin, R.H.2
-
8
-
-
0025780140
-
Chromosome abnormalities in human spermatozoa after albumin or TEST yolk capacitation
-
Benet J, Navarro J, Genescà A, Egozcue J, Templado C (1991) Chromosome abnormalities in human spermatozoa after albumin or TEST yolk capacitation. Hum Reprod 6 : 369-375
-
(1991)
Hum Reprod
, vol.6
, pp. 369-375
-
-
Benet, J.1
Navarro, J.2
Genescà, A.3
Egozcue, J.4
Templado, C.5
-
9
-
-
0026585738
-
Cytogenetic studies in motile sperm from normal men
-
Benet J, Genescà A, Navarro J, Egozcue J, Templado C (1992) Cytogenetic studies in motile sperm from normal men. Hum Genet 89 : 176-180
-
(1992)
Hum Genet
, vol.89
, pp. 176-180
-
-
Benet, J.1
Genescà, A.2
Navarro, J.3
Egozcue, J.4
Templado, C.5
-
10
-
-
0028610098
-
Chromosome aberrations in normal and translocated human sperm: Role in reproduction pathology
-
Benkhalifa M, Malet P, Qumsiyeh MB, Boucher D, Bellec V, Menezo Y (1994) Chromosome aberrations in normal and translocated human sperm: role in reproduction pathology. Rev Fr Gynecol Obstet 2 : 288-296
-
(1994)
Rev Fr Gynecol Obstet
, vol.2
, pp. 288-296
-
-
Benkhalifa, M.1
Malet, P.2
Qumsiyeh, M.B.3
Boucher, D.4
Bellec, V.5
Menezo, Y.6
-
11
-
-
0028212715
-
Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm
-
Bischoff FZ, Nguyen DD, Burt KJ, Shaffer LG (1994) Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenet Cell Genet 66 : 237-243
-
(1994)
Cytogenet Cell Genet
, vol.66
, pp. 237-243
-
-
Bischoff, F.Z.1
Nguyen, D.D.2
Burt, K.J.3
Shaffer, L.G.4
-
12
-
-
0029985631
-
Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent insitu hybridization
-
Blanco J, Egozcue J, Vidal F (1996) Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent insitu hybridization. Hum Reprod 11 : 722-726
-
(1996)
Hum Reprod
, vol.11
, pp. 722-726
-
-
Blanco, J.1
Egozcue, J.2
Vidal, F.3
-
13
-
-
0015525065
-
Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9
-
Bobrow M, Madan K, Pearson PL (1972) Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9. Nature 238 : 122-124
-
(1972)
Nature
, vol.238
, pp. 122-124
-
-
Bobrow, M.1
Madan, K.2
Pearson, P.L.3
-
14
-
-
0021229266
-
Collaborative study of the segregation of inherited chromosome structural rearrangements in 1,356 prenatal diagnosis
-
Boué A, Gallano P (1984) Collaborative study of the segregation of inherited chromosome structural rearrangements in 1,356 prenatal diagnosis. Prenat Diagn 4 : 45-67
-
(1984)
Prenat Diagn
, vol.4
, pp. 45-67
-
-
Boué, A.1
Gallano, P.2
-
15
-
-
0021323170
-
Chromosomal abnormalities in human sperm: Comparisons among four healthy men
-
Brandriff B, Gordon L, Ashworth L, Watchmaker G, Carrano A, Wyrobek A (1984) Chromosomal abnormalities in human sperm: comparisons among four healthy men. Hum Genet 66 : 193-201
-
(1984)
Hum Genet
, vol.66
, pp. 193-201
-
-
Brandriff, B.1
Gordon, L.2
Ashworth, L.3
Watchmaker, G.4
Carrano, A.5
Wyrobek, A.6
-
16
-
-
0021908105
-
Chromosomes of human sperm: Variability among normal individuals
-
Brandriff B, Gordon L, Ashworth L, Watchmaker G, Moore D II, Wyrobek AJ, Carrano A (1985) Chromosomes of human sperm: variability among normal individuals. Hum Genet 70 : 18-24
-
(1985)
Hum Genet
, vol.70
, pp. 18-24
-
-
Brandriff, B.1
Gordon, L.2
Ashworth, L.3
Watchmaker, G.4
Moore II, D.5
Wyrobek, A.J.6
Carrano, A.7
-
17
-
-
0022504805
-
Cytogenetics of human sperm: Meiotic segregation in two translocation carriers
-
Brandriff B, Gordon L, Ashworth LK, Littman V, Watchmaker G, Carrano AV (1986a) Cytogenetics of human sperm: meiotic segregation in two translocation carriers. Am J Hum Genet 38 : 197-208
-
(1986)
Am J Hum Genet
, vol.38
, pp. 197-208
-
-
Brandriff, B.1
Gordon, L.2
Ashworth, L.K.3
Littman, V.4
Watchmaker, G.5
Carrano, A.V.6
-
18
-
-
0023027048
-
The chromosomal constitution of human sperm selected for motility
-
Brandriff BF, Gordon LA, Haendel S, Ashworth LK, Carrano AV (1986b) The chromosomal constitution of human sperm selected for motility. Fertil Steril 46 : 686-690
-
(1986)
Fertil Steril
, vol.46
, pp. 686-690
-
-
Brandriff, B.F.1
Gordon, L.A.2
Haendel, S.3
Ashworth, L.K.4
Carrano, A.V.5
-
20
-
-
0028040273
-
Chromosomal damage in sperm of patients surviving Hodgkin's disease following MOPP (nitrogen mustard, vincristine, procarbazine, and prednisone) therapy with and without radiotherapy
-
Brandriff BF, Meistrich ML, Gordon LA, Carrano AV, Liang JC (1994) Chromosomal damage in sperm of patients surviving Hodgkin's disease following MOPP (nitrogen mustard, vincristine, procarbazine, and prednisone) therapy with and without radiotherapy. Hum Genet 93 : 295-299
-
(1994)
Hum Genet
, vol.93
, pp. 295-299
-
-
Brandriff, B.F.1
Meistrich, M.L.2
Gordon, L.A.3
Carrano, A.V.4
Liang, J.C.5
-
21
-
-
0022492342
-
Analysis of meiotic segregation in a man heterozygous for two reciprocal translocations using the hamster in vitro penetration system
-
Burns JP, Koduru PRK, Alonso ML, Chaganti RSK (1986) Analysis of meiotic segregation in a man heterozygous for two reciprocal translocations using the hamster in vitro penetration system. Am J Hum Genet 38 : 954-964
-
(1986)
Am J Hum Genet
, vol.38
, pp. 954-964
-
-
Burns, J.P.1
Koduru, P.R.K.2
Alonso, M.L.3
Chaganti, R.S.K.4
-
22
-
-
0016713572
-
The recognition and incidence of haploid and polyploid spermatozoa in man, rabbit and mouse
-
Carothers AD, Beatty RA (1975) The recognition and incidence of haploid and polyploid spermatozoa in man, rabbit and mouse. J Reprod Fertil 44 : 487-500
-
(1975)
J Reprod Fertil
, vol.44
, pp. 487-500
-
-
Carothers, A.D.1
Beatty, R.A.2
-
23
-
-
0027971311
-
Male meiotic segregation of gonosomes analysed by two-color FISH in human interphase spermatozoa
-
Chevret E, Rousseaux S, Monteil M, Cozzi J, Pelletier R, Mollard J, Sèle B (1994) Male meiotic segregation of gonosomes analysed by two-color FISH in human interphase spermatozoa. Hum Genet 94 : 701-704
-
(1994)
Hum Genet
, vol.94
, pp. 701-704
-
-
Chevret, E.1
Rousseaux, S.2
Monteil, M.3
Cozzi, J.4
Pelletier, R.5
Mollard, J.6
Sèle, B.7
-
24
-
-
0029147570
-
Meiotic segregation of the X and Y chromosomes and chromosome 1 analyzed by three-color FISH in human interphase spermatozoa
-
Chevret E, Rousseaux S, Monteil M, Pelletier R, Cozzi J, Sèle B (1995) Meiotic segregation of the X and Y chromosomes and chromosome 1 analyzed by three-color FISH in human interphase spermatozoa. Cytogenet Cell Genet 71 : 126-130
-
(1995)
Cytogenet Cell Genet
, vol.71
, pp. 126-130
-
-
Chevret, E.1
Rousseaux, S.2
Monteil, M.3
Pelletier, R.4
Cozzi, J.5
Sèle, B.6
-
25
-
-
0029815731
-
Double and triple in situ chromosomal labeling of human spermatozoa by PRINS
-
Coignet L, Girardet A, Andréo B, Charlieu JP, Pellestor F (1996) Double and triple in situ chromosomal labeling of human spermatozoa by PRINS. Cytogenet Cell Genet 73 : 300-303
-
(1996)
Cytogenet Cell Genet
, vol.73
, pp. 300-303
-
-
Coignet, L.1
Girardet, A.2
Andréo, B.3
Charlieu, J.P.4
Pellestor, F.5
-
26
-
-
0025974026
-
Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa
-
Coonen E, Pieters MHEC, Dumoulin JCM, Meyer H, Evers JLH, Ramaekers FCS, Geraedts JPM (1991) Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa. Mol Reprod Dev 28 : 18-22
-
(1991)
Mol Reprod Dev
, vol.28
, pp. 18-22
-
-
Coonen, E.1
Pieters, M.2
Dumoulin, J.C.M.3
Meyer, H.4
Evers, J.L.H.5
Ramaekers, F.C.S.6
Geraedts, J.P.M.7
-
27
-
-
0028158533
-
Achievement of meiosis in XXY germ cells: Study of 543 sperm karyotypes from an XY/XXY mosaic patient
-
Cozzi J, Chevret E, Rousseaux S, Pelletier R, Benitz V, Jalbert H, Sèle B (1994) Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient. Hum Genet 93 : 32-34
-
(1994)
Hum Genet
, vol.93
, pp. 32-34
-
-
Cozzi, J.1
Chevret, E.2
Rousseaux, S.3
Pelletier, R.4
Benitz, V.5
Jalbert, H.6
Sèle, B.7
-
28
-
-
0019249207
-
Higher risk to D;G-translocation carriers of t dic(13;21) as compared to t dic(14;21)
-
Daniel A, Williams K, Lam-Po-Tang PRLC (1980) Higher risk to D;G-translocation carriers of t dic(13;21) as compared to t dic(14;21). J Med Genet 17 : 491-492
-
(1980)
J Med Genet
, vol.17
, pp. 491-492
-
-
Daniel, A.1
Williams, K.2
Lam-Po-Tang, P.R.L.C.3
-
29
-
-
0025784570
-
Cytogenetic studies in human sperm
-
Estop AM, Cieply K, Vankirk V, Munné S, Garver K (1991) Cytogenetic studies in human sperm. Hum Genet 87 : 447-451
-
(1991)
Hum Genet
, vol.87
, pp. 447-451
-
-
Estop, A.M.1
Cieply, K.2
Vankirk, V.3
Munné, S.4
Garver, K.5
-
30
-
-
0026635246
-
The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation
-
Estop AM, Levinson F, Cieply K, Vankirk V (1992) The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation. Hum Genet 89 : 425-429
-
(1992)
Hum Genet
, vol.89
, pp. 425-429
-
-
Estop, A.M.1
Levinson, F.2
Cieply, K.3
Vankirk, V.4
-
31
-
-
0028887505
-
An analysis of human sperm chromosome breakpoints
-
Estop AM, Márquez C, Munné S, Navarro J, Cieply K, Van Kirk V, Martorell MR, Benet J, Templado C (1995a) An analysis of human sperm chromosome breakpoints. Am J Hum Genet 56 : 452-460
-
(1995)
Am J Hum Genet
, vol.56
, pp. 452-460
-
-
Estop, A.M.1
Márquez, C.2
Munné, S.3
Navarro, J.4
Cieply, K.5
Van Kirk, V.6
Martorell, M.R.7
Benet, J.8
Templado, C.9
-
32
-
-
0028946651
-
Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literature
-
Estop AM, Vankirk V, Cieply K (1995b) Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literature. Cytogenet Cell Genet 70 : 80-87
-
(1995)
Cytogenet Cell Genet
, vol.70
, pp. 80-87
-
-
Estop, A.M.1
Vankirk, V.2
Cieply, K.3
-
33
-
-
0027440975
-
Molecular studies of trisomy 18
-
Fisher JM, Harvey JF, Lindenbaum RH, Boyd PA, Jacobs PA (1993) Molecular studies of trisomy 18. Am J Hum Genet 52 : 1139-1144
-
(1993)
Am J Hum Genet
, vol.52
, pp. 1139-1144
-
-
Fisher, J.M.1
Harvey, J.F.2
Lindenbaum, R.H.3
Boyd, P.A.4
Jacobs, P.A.5
-
34
-
-
1842339762
-
Chromosome displacement hypothesis
-
Vig BK, Sandberg AA (eds) Liss, New York
-
Ford JH (1987) Chromosome displacement hypothesis. In: Vig BK, Sandberg AA (eds) Aneuploidy. Part A. Incidence and etiology. Liss, New York, pp 237-247
-
(1987)
Aneuploidy. Part A. Incidence and Etiology
, pp. 237-247
-
-
Ford, J.H.1
-
35
-
-
0025334239
-
Human sperm chromosomes. Long-term effect of cancer treatment
-
Genescà A, Caballín MR, Miró R, Benet J, Bonfill X, Egozcue J (1990) Human sperm chromosomes. Long-term effect of cancer treatment. Cancer Genet Cytogenet 46 : 251-260
-
(1990)
Cancer Genet Cytogenet
, vol.46
, pp. 251-260
-
-
Genescà, A.1
Caballín, M.R.2
Miró, R.3
Benet, J.4
Bonfill, X.5
Egozcue, J.6
-
36
-
-
0015899204
-
Specific staining of the human No. 1 chromosome in spermatozoa
-
Geraedts J, Pearson P (1973) Specific staining of the human No. 1 chromosome in spermatozoa. Hum Genet 20 : 171-173
-
(1973)
Hum Genet
, vol.20
, pp. 171-173
-
-
Geraedts, J.1
Pearson, P.2
-
37
-
-
0016688458
-
Spatial distribution of chromosomes 1 and Y in human spermatozoa
-
Geraedts JPM, Pearson PL (1975) Spatial distribution of chromosomes 1 and Y in human spermatozoa. J Reprod Fertil 45 : 515-517
-
(1975)
J Reprod Fertil
, vol.45
, pp. 515-517
-
-
Geraedts, J.P.M.1
Pearson, P.L.2
-
38
-
-
0029815984
-
Aneuploidy detection in human sperm nuclei using PRINS technique
-
Girardet A, Coignet L, Andréo B, Lefort G, Charlieu JP, Pellestor F (1996) Aneuploidy detection in human sperm nuclei using PRINS technique. Am J Med Genet 64 : 488-492
-
(1996)
Am J Med Genet
, vol.64
, pp. 488-492
-
-
Girardet, A.1
Coignet, L.2
Andréo, B.3
Lefort, G.4
Charlieu, J.P.5
Pellestor, F.6
-
39
-
-
0027793248
-
Analysis of the primary sex ratio, sex chromosome aneuploidy and diploidy in human sperm using dual-colour fluorescence in situ hybridization
-
Goldman ASH, Fomina Z, Knights PA, Hill CJ, Walker AP, Hultén MA (1993) Analysis of the primary sex ratio, sex chromosome aneuploidy and diploidy in human sperm using dual-colour fluorescence in situ hybridization. Eur J Hum Genet 1 : 325-334
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 325-334
-
-
Goldman, A.S.H.1
Fomina, Z.2
Knights, P.A.3
Hill, C.J.4
Walker, A.P.5
Hultén, M.A.6
-
40
-
-
0028792586
-
Non-disjunction in human sperm: Evidence for an effect of increasing paternal age
-
Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ (1995) Non-disjunction in human sperm: evidence for an effect of increasing paternal age. Hum Mol Genet 4 : 2227-2232
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2227-2232
-
-
Griffin, D.K.1
Abruzzo, M.A.2
Millie, E.A.3
Sheean, L.A.4
Feingold, E.5
Sherman, S.L.6
Hassold, T.J.7
-
41
-
-
0022532840
-
Pericentric inversions in man. A French collaborative study
-
Groupe de Cytogénéticiens Français (1986) Pericentric inversions in man. A French collaborative study. Ann Genet 29 : 129-176
-
(1986)
Ann Genet
, vol.29
, pp. 129-176
-
-
-
42
-
-
0025359715
-
Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridization
-
Guttenbach M, Schmid M (1990) Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridization. Am J Hum Genet 46 : 553-558
-
(1990)
Am J Hum Genet
, vol.46
, pp. 553-558
-
-
Guttenbach, M.1
Schmid, M.2
-
43
-
-
0025864454
-
Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei
-
Guttenbach M, Schmid M (1991) Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei. Hum Genet 87 : 261-265
-
(1991)
Hum Genet
, vol.87
, pp. 261-265
-
-
Guttenbach, M.1
Schmid, M.2
-
44
-
-
0028055197
-
Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradioactive in situ hybridization
-
Guttenbach M, Schakowski R, Schmid M (1994a) Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradioactive in situ hybridization. Hum Genet 93 : 7-12
-
(1994)
Hum Genet
, vol.93
, pp. 7-12
-
-
Guttenbach, M.1
Schakowski, R.2
Schmid, M.3
-
45
-
-
0028327204
-
Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization
-
Guttenbach M, Schakowski R, Schmid M (1994b) Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization. Hum Genet 93 : 421-423
-
(1994)
Hum Genet
, vol.93
, pp. 421-423
-
-
Guttenbach, M.1
Schakowski, R.2
Schmid, M.3
-
46
-
-
1842298135
-
Incidence of diploid and disomic sperm nuclei in 45 infertile men
-
Guttenbach M, Martinez-Expósito MJ, Michelmann HW, Engel W, Schmid M (1997a) Incidence of diploid and disomic sperm nuclei in 45 infertile men. Hum Reprod 12 : 468-473
-
(1997)
Hum Reprod
, vol.12
, pp. 468-473
-
-
Guttenbach, M.1
Martinez-Expósito, M.J.2
Michelmann, H.W.3
Engel, W.4
Schmid, M.5
-
47
-
-
0030896411
-
Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's syndrome: A FISH analysis
-
Guttenbach M, Michelmann HW, Hinney B, Engel W, Schmid M (1997b) Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's syndrome: a FISH analysis. Hum Genet 99 : 474-477
-
(1997)
Hum Genet
, vol.99
, pp. 474-477
-
-
Guttenbach, M.1
Michelmann, H.W.2
Hinney, B.3
Engel, W.4
Schmid, M.5
-
48
-
-
0026722597
-
Detection of chromosome 17- and X-bearing human spermatozoa using fluorescence in situ hybridization
-
Han TL, Webb GC, Flaherty SP, Correll A, Matthews CD, Ford JH (1992) Detection of chromosome 17- and X-bearing human spermatozoa using fluorescence in situ hybridization. Mol Reprod Dev 33 : 189-194
-
(1992)
Mol Reprod Dev
, vol.33
, pp. 189-194
-
-
Han, T.L.1
Webb, G.C.2
Flaherty, S.P.3
Correll, A.4
Matthews, C.D.5
Ford, J.H.6
-
49
-
-
0027456565
-
Simultaneous detection of X- and Y-bearing human sperm by double fluorescence in situ hybridization
-
Han TL, Ford JH, Webb GC, Flaherty SP, Correll A, Matthews CD (1993) Simultaneous detection of X- and Y-bearing human sperm by double fluorescence in situ hybridization. Mol Reprod Dev 34 : 308-313
-
(1993)
Mol Reprod Dev
, vol.34
, pp. 308-313
-
-
Han, T.L.1
Ford, J.H.2
Webb, G.C.3
Flaherty, S.P.4
Correll, A.5
Matthews, C.D.6
-
50
-
-
0000049938
-
Chromosomal abnormalities in human reproductive wastage
-
Hassold TJ (1986) Chromosomal abnormalities in human reproductive wastage. Trends Genet 2 : 105-110
-
(1986)
Trends Genet
, vol.2
, pp. 105-110
-
-
Hassold, T.J.1
-
51
-
-
0023930140
-
Cytogenetic and molecular analysis of sex chromosome monosomy
-
Hassold T, Benham F, Leppert M (1988) Cytogenetic and molecular analysis of sex chromosome monosomy. Am J Hum Genet 42 : 534-541
-
(1988)
Am J Hum Genet
, vol.42
, pp. 534-541
-
-
Hassold, T.1
Benham, F.2
Leppert, M.3
-
52
-
-
0001815697
-
Aneuploidy in humans: Dimensions, demography, and dangers of abnormal numbers of chromosomes
-
Vig BK, Sandberg AA (eds) Liss, New York
-
Hecht F, Hecht BK (1987) Aneuploidy in humans: dimensions, demography, and dangers of abnormal numbers of chromosomes. In: Vig BK, Sandberg AA (eds) Aneuploidy. Part A. Incidence and etiology. Liss, New York, pp 9-49
-
(1987)
Aneuploidy. Part A. Incidence and Etiology
, pp. 9-49
-
-
Hecht, F.1
Hecht, B.K.2
-
53
-
-
0027406691
-
Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization
-
Holmes JM, Martin RH (1993) Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization. Hum Genet 91 : 20-24
-
(1993)
Hum Genet
, vol.91
, pp. 20-24
-
-
Holmes, J.M.1
Martin, R.H.2
-
54
-
-
1842411168
-
Segregation analysis of balanced pericentric inversions in pedigree data
-
Iselius L, Sherman S, Gallano P, Buckton K, Collyer S, Demey R, Kristoffersson U, Lindsten J, Mikkelsen M, Morton N, Newton M, Nordensson I, Petersen M, Wahlstrom J (1985) Segregation analysis of balanced pericentric inversions in pedigree data. Am J Hum Genet 37 : A98
-
(1985)
Am J Hum Genet
, vol.37
-
-
Iselius, L.1
Sherman, S.2
Gallano, P.3
Buckton, K.4
Collyer, S.5
Demey, R.6
Kristoffersson, U.7
Lindsten, J.8
Mikkelsen, M.9
Morton, N.10
Newton, M.11
Nordensson, I.12
Petersen, M.13
Wahlstrom, J.14
-
55
-
-
0002958784
-
Estimation of aneuploidy levels in human spermatozoa using chromosome complements and chromosome specific probes
-
Jackson-Cook C, Haller VL (1991) Estimation of aneuploidy levels in human spermatozoa using chromosome complements and chromosome specific probes. Am J Hum Genet 49 : A18
-
(1991)
Am J Hum Genet
, vol.49
-
-
Jackson-Cook, C.1
Haller, V.L.2
-
56
-
-
0023682678
-
Klinefelter's syndrome: An analysis of the origin of the additional sex chromosome using molecular probes
-
Jacobs P, Hassold T, Whittington E, Butler G, Collier S, Keston M, Lee M (1988) Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes. Ann Hum Genet 52 : 93-109
-
(1988)
Ann Hum Genet
, vol.52
, pp. 93-109
-
-
Jacobs, P.1
Hassold, T.2
Whittington, E.3
Butler, G.4
Collier, S.5
Keston, M.6
Lee, M.7
-
57
-
-
0026794326
-
Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and a t(3;8)(p13;p21) reciprocal translocation
-
Jenderny J (1992) Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and a t(3;8)(p13;p21) reciprocal translocation. Hum Genet 90 : 171-173
-
(1992)
Hum Genet
, vol.90
, pp. 171-173
-
-
Jenderny, J.1
-
58
-
-
0023263285
-
Chromosome analysis of human sperm. I. First results with a modified method
-
Jenderny J, Röhrborn G (1987) Chromosome analysis of human sperm. I. First results with a modified method. Hum Genet 76 : 385-388
-
(1987)
Hum Genet
, vol.76
, pp. 385-388
-
-
Jenderny, J.1
Röhrborn, G.2
-
59
-
-
0026545030
-
Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20
-
Jenderny J, Gebauer J, Röhrborn G, Rüger A (1992a) Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20. Hum Genet 89 : 117-119
-
(1992)
Hum Genet
, vol.89
, pp. 117-119
-
-
Jenderny, J.1
Gebauer, J.2
Röhrborn, G.3
Rüger, A.4
-
60
-
-
0026801137
-
Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patients
-
Jenderny J, Jacobi ML, Rüger A, Röhrborn G (1992b) Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patients. Hum Genet 10 : 151-154
-
(1992)
Hum Genet
, vol.10
, pp. 151-154
-
-
Jenderny, J.1
Jacobi, M.L.2
Rüger, A.3
Röhrborn, G.4
-
61
-
-
0021351337
-
Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridization
-
Joseph AM, Gosden JR, Chandley AC (1984) Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridization. Hum Genet 66 : 234-238
-
(1984)
Hum Genet
, vol.66
, pp. 234-238
-
-
Joseph, A.M.1
Gosden, J.R.2
Chandley, A.C.3
-
62
-
-
0021710068
-
Pericentric inversions. Problems and significance for clinical genetics
-
Kaiser P (1984) Pericentric inversions. Problems and significance for clinical genetics. Hum Genet 68 : 1-47
-
(1984)
Hum Genet
, vol.68
, pp. 1-47
-
-
Kaiser, P.1
-
63
-
-
0022499685
-
An improved, efficient method for analyzing human sperm chromosomes using zona-free hamster ova
-
Kamiguchi Y, Mikamo K (1986) An improved, efficient method for analyzing human sperm chromosomes using zona-free hamster ova. Am J Hum Genet 38 : 724-740
-
(1986)
Am J Hum Genet
, vol.38
, pp. 724-740
-
-
Kamiguchi, Y.1
Mikamo, K.2
-
64
-
-
0019792517
-
An improved method for Y-body identification and confirmation of a high incidence of YY sperm nuclei
-
Klasen M, Schmid M (1981) An improved method for Y-body identification and confirmation of a high incidence of YY sperm nuclei. Hum Genet 58 : 156-161
-
(1981)
Hum Genet
, vol.58
, pp. 156-161
-
-
Klasen, M.1
Schmid, M.2
-
65
-
-
0023105275
-
Pericentric inversions in man: Personal experience and review of the literature
-
Kleczkowska A, Fryns JP, Van den Berghe (1987) Pericentric inversions in man: personal experience and review of the literature. Hum Genet 75 : 333-338
-
(1987)
Hum Genet
, vol.75
, pp. 333-338
-
-
Kleczkowska, A.1
Fryns, J.P.2
Van Berghe, D.3
-
66
-
-
0001752958
-
Autosomal disorders
-
Lejeune J (1963) Autosomal disorders. Pediatrics 32 : 326-337
-
(1963)
Pediatrics
, vol.32
, pp. 326-337
-
-
Lejeune, J.1
-
67
-
-
0027992136
-
Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8)(q23;q27;p21)
-
Lu PY, Hammit DG, Zinsmeister AR, Dewald GW (1994) Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8)(q23;q27;p21). Fertil Steril 62 : 394-399
-
(1994)
Fertil Steril
, vol.62
, pp. 394-399
-
-
Lu, P.Y.1
Hammit, D.G.2
Zinsmeister, A.R.3
Dewald, G.W.4
-
69
-
-
0021344378
-
Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation, t(11;22)(q23;q11)
-
Martin RH (1984) Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation, t(11;22)(q23;q11). Clin Genet 25 : 357-361
-
(1984)
Clin Genet
, vol.25
, pp. 357-361
-
-
Martin, R.H.1
-
70
-
-
0022451865
-
Sperm chromosome analysis in a man heterozygous for a paracentric inversion of chromosome 7(q11q22)
-
Martin RH (1986) Sperm chromosome analysis in a man heterozygous for a paracentric inversion of chromosome 7(q11q22). Hum Genet 73 : 97-100
-
(1986)
Hum Genet
, vol.73
, pp. 97-100
-
-
Martin, R.H.1
-
71
-
-
0024230620
-
Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation
-
Martin RH (1988a) Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation. Hum Genet 80 : 357-361
-
(1988)
Hum Genet
, vol.80
, pp. 357-361
-
-
Martin, R.H.1
-
72
-
-
0023942870
-
Meiotic segregation of human sperm chromosomes in translocation heterozygotes: Report of a t(9,10)(q34;q11) and a review of the literature
-
Martin RH (1988b) Meiotic segregation of human sperm chromosomes in translocation heterozygotes: report of a t(9,10)(q34;q11) and a review of the literature. Cytogenet Cell Genet 47 : 48-51
-
(1988)
Cytogenet Cell Genet
, vol.47
, pp. 48-51
-
-
Martin, R.H.1
-
73
-
-
0025794297
-
Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion, inv(3)(p25q21)
-
Martin RH (1991) Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion, inv(3)(p25q21). Am J Hum Genet 48 : 856-861
-
(1991)
Am J Hum Genet
, vol.48
, pp. 856-861
-
-
Martin, R.H.1
-
74
-
-
0026583150
-
Sperm chromosome analysis of two men heterozygous for reciprocal translocations: T(1;9)(q22;q31) and t(16;19)(q11.1;q13.3)
-
Martin RH (1992) Sperm chromosome analysis of two men heterozygous for reciprocal translocations: t(1;9)(q22;q31) and t(16;19)(q11.1;q13.3). Cytogenet Cell Genet 60 : 18-21
-
(1992)
Cytogenet Cell Genet
, vol.60
, pp. 18-21
-
-
Martin, R.H.1
-
75
-
-
0027399169
-
Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion, inv(8)(p23q22)
-
Martin RH (1993) Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion, inv(8)(p23q22). Cytogenet Cell Genet 62 : 199-202
-
(1993)
Cytogenet Cell Genet
, vol.62
, pp. 199-202
-
-
Martin, R.H.1
-
76
-
-
0027983821
-
Sperm chromosome complements in a man heterozygous for a reciprocal translocation t(2;3)(q24;p26)
-
Martin RH (1994) Sperm chromosome complements in a man heterozygous for a reciprocal translocation t(2;3)(q24;p26). Hum Reprod 9 : 1512-1515
-
(1994)
Hum Reprod
, vol.9
, pp. 1512-1515
-
-
Martin, R.H.1
-
77
-
-
0027155211
-
Chromosome complements in 695 sperm from three men heterozygous for reciprocal translocations, and a review of the literature
-
Martin RH, Hultén M (1993) Chromosome complements in 695 sperm from three men heterozygous for reciprocal translocations, and a review of the literature. Hereditas 118 : 165-175
-
(1993)
Hereditas
, vol.118
, pp. 165-175
-
-
Martin, R.H.1
Hultén, M.2
-
78
-
-
0023577485
-
The effect of age on the frequency of sperm chromosomal abnormalities in normal men
-
Martin RH, Rademaker AW (1987) The effect of age on the frequency of sperm chromosomal abnormalities in normal men. Am J Hum Genet 41 : 484-492
-
(1987)
Am J Hum Genet
, vol.41
, pp. 484-492
-
-
Martin, R.H.1
Rademaker, A.W.2
-
79
-
-
0023904370
-
The relationship between sperm chromosomal abnormalities and sperm morphology in humans
-
Martin RH, Rademaker AW (1988) The relationship between sperm chromosomal abnormalities and sperm morphology in humans. Mutat Res 207 : 159-164
-
(1988)
Mutat Res
, vol.207
, pp. 159-164
-
-
Martin, R.H.1
Rademaker, A.W.2
-
80
-
-
0025331172
-
The frequency of aneuploidy among individual chromosomes in 6,821 human sperm chromosome complements
-
Martin RH, Rademaker AW (1990) The frequency of aneuploidy among individual chromosomes in 6,821 human sperm chromosome complements. Cytogenet Cell Genet 53 : 103-107
-
(1990)
Cytogenet Cell Genet
, vol.53
, pp. 103-107
-
-
Martin, R.H.1
Rademaker, A.W.2
-
81
-
-
0029134776
-
Reliability of aneuploidy estimates in human sperm: Results of fluorescence in situ hybridization studies using two different scoring criteria
-
Martin RH, Rademaker AW (1995) Reliability of aneuploidy estimates in human sperm: results of fluorescence in situ hybridization studies using two different scoring criteria. Mol Reprod Dev 42 : 89-93
-
(1995)
Mol Reprod Dev
, vol.42
, pp. 89-93
-
-
Martin, R.H.1
Rademaker, A.W.2
-
82
-
-
0028855742
-
Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY, t(9;13)(q21.1;q21.2) and a review of the literature
-
Martin RH, Spriggs EL (1995) Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY, t(9;13)(q21.1;q21.2) and a review of the literature. Clin Genet 47 : 42-46
-
(1995)
Clin Genet
, vol.47
, pp. 42-46
-
-
Martin, R.H.1
Spriggs, E.L.2
-
83
-
-
0020051046
-
Direct chromosomal analysis of human spermatozoa: Preliminary results from 18 normal men
-
Martin RH, Lin CC, Balkan W, Burns K (1982) Direct chromosomal analysis of human spermatozoa: preliminary results from 18 normal men. Am J Hum Genet 34 : 459-468
-
(1982)
Am J Hum Genet
, vol.34
, pp. 459-468
-
-
Martin, R.H.1
Lin, C.C.2
Balkan, W.3
Burns, K.4
-
84
-
-
0020608012
-
The chromosome constitution of 1000 human spermatozoa
-
Martin RH, Balkan W, Burns K, Rademaker AW, Lin CC, Rudd NL (1983) The chromosome constitution of 1000 human spermatozoa. Hum Genet 63 : 305-309
-
(1983)
Hum Genet
, vol.63
, pp. 305-309
-
-
Martin, R.H.1
Balkan, W.2
Burns, K.3
Rademaker, A.W.4
Lin, C.C.5
Rudd, N.L.6
-
85
-
-
0023629482
-
Variation in the frequency and type of sperm chromosomal abnormalities among normal men
-
Martin RH, Rademaker AW, Hildebrand K, Long-Simpson L, Peterson D, Yamamoto J (1987) Variation in the frequency and type of sperm chromosomal abnormalities among normal men. Hum Genet 77 : 108-114
-
(1987)
Hum Genet
, vol.77
, pp. 108-114
-
-
Martin, R.H.1
Rademaker, A.W.2
Hildebrand, K.3
Long-Simpson, L.4
Peterson, D.5
Yamamoto, J.6
-
86
-
-
0025201998
-
Cytogenetic analysis of 400 sperm from three translocation heterozygotes
-
Martin RH, Barclay L, Hildebrand K, Ko E, Fowlow SB (1990a) Cytogenetic analysis of 400 sperm from three translocation heterozygotes. Hum Genet 86 : 33-39
-
(1990)
Hum Genet
, vol.86
, pp. 33-39
-
-
Martin, R.H.1
Barclay, L.2
Hildebrand, K.3
Ko, E.4
Fowlow, S.B.5
-
87
-
-
0025063097
-
Sperm chromosome analysis in a man heterozygous for a reciprocal translocation, 46,XY,t(12;20)(q24.3;q11)
-
Martin RH, McGillivray B, Barclay L, Hildebrand K, Ko E (1990 b) Sperm chromosome analysis in a man heterozygous for a reciprocal translocation, 46,XY,t(12;20)(q24.3;q11). Hum Reprod 5 : 606-609
-
(1990)
Hum Reprod
, vol.5
, pp. 606-609
-
-
Martin, R.H.1
McGillivray, B.2
Barclay, L.3
Hildebrand, K.4
Ko, E.5
-
88
-
-
0025293350
-
The effect of culture conditions and media on the frequency of chromosomal abnormalities in human sperm chromosome complements
-
Martin RH, Templado C, Ko E, Rademaker A (1990c) The effect of culture conditions and media on the frequency of chromosomal abnormalities in human sperm chromosome complements. Mol Reprod Dev 26 : 101-104
-
(1990)
Mol Reprod Dev
, vol.26
, pp. 101-104
-
-
Martin, R.H.1
Templado, C.2
Ko, E.3
Rademaker, A.4
-
89
-
-
0025853757
-
Distribution of aneuploidy in human gametes: Comparison between human sperm and oocytes
-
Martin RH, Ko E, Rademaker AW (1991) Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes. Am J Med Genet 39 : 321-331
-
(1991)
Am J Med Genet
, vol.39
, pp. 321-331
-
-
Martin, R.H.1
Ko, E.2
Rademaker, A.W.3
-
90
-
-
0026752917
-
Analysis of sperm chromosome complements from a man heterozygous for a Robertsonian translocation 45,XY,t(15q;22q)
-
Martin RH, Ko E, Hildebrand K (1992a) Analysis of sperm chromosome complements from a man heterozygous for a Robertsonian translocation 45,XY,t(15q;22q). Am J Med Genet 43 : 855-857
-
(1992)
Am J Med Genet
, vol.43
, pp. 855-857
-
-
Martin, R.H.1
Ko, E.2
Hildebrand, K.3
-
91
-
-
0026665564
-
A comparison of the frequency and type of chromosomal abnormalities in human sperm after different capacitation conditions
-
Martin RH, Rademaker AW, Ko E, Barclay L, Hildebrand K (1992 b) A comparison of the frequency and type of chromosomal abnormalities in human sperm after different capacitation conditions. Biol Reprod 47 : 268-270
-
(1992)
Biol Reprod
, vol.47
, pp. 268-270
-
-
Martin, R.H.1
Rademaker, A.W.2
Ko, E.3
Barclay, L.4
Hildebrand, K.5
-
92
-
-
0027326143
-
Detection of aneuploidy in human interphase spermatozoa by fluorescence in situ hybridization (FISH)
-
Martin RH, Ko E, Chan K (1993) Detection of aneuploidy in human interphase spermatozoa by fluorescence in situ hybridization (FISH). Cytogenet Cell Genet 64 : 23-26
-
(1993)
Cytogenet Cell Genet
, vol.64
, pp. 23-26
-
-
Martin, R.H.1
Ko, E.2
Chan, K.3
-
93
-
-
0028118866
-
Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1
-
Martin RH, Chernos JE, Lowry RB, Pattinson HA, Barclay L, Ko E (1994) Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1. Hum Genet 93 : 135-138
-
(1994)
Hum Genet
, vol.93
, pp. 135-138
-
-
Martin, R.H.1
Chernos, J.E.2
Lowry, R.B.3
Pattinson, H.A.4
Barclay, L.5
Ko, E.6
-
94
-
-
0028958781
-
Analysis of chromosome abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH)
-
Martin RH, Rademaker AW, Leonard NJ (1995a) Analysis of chromosome abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH). Cancer Genet Cytogenet 80 : 29-32
-
(1995)
Cancer Genet Cytogenet
, vol.80
, pp. 29-32
-
-
Martin, R.H.1
Rademaker, A.W.2
Leonard, N.J.3
-
95
-
-
0028818839
-
The relationship between paternal age, sex ratios, and aneuploidy frequencies in human sperm, as assessed by multicolor FISH
-
Martin RH, Spriggs E, Ko E, Rademaker AW (1995b) The relationship between paternal age, sex ratios, and aneuploidy frequencies in human sperm, as assessed by multicolor FISH. Am J Hum Genet 57 : 1395-1399
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1395-1399
-
-
Martin, R.H.1
Spriggs, E.2
Ko, E.3
Rademaker, A.W.4
-
96
-
-
0028269490
-
Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization
-
Miharu N, Best RG, Young SR (1994) Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization. Hum Genet 93 : 502-506
-
(1994)
Hum Genet
, vol.93
, pp. 502-506
-
-
Miharu, N.1
Best, R.G.2
Young, S.R.3
-
97
-
-
0029087947
-
Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization
-
Moosani N, Pattinson HA, Carter MD, Cox DM, Rademaker AW, Martin RH (1995) Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization. Fertil Steril 64 : 811-817
-
(1995)
Fertil Steril
, vol.64
, pp. 811-817
-
-
Moosani, N.1
Pattinson, H.A.2
Carter, M.D.3
Cox, D.M.4
Rademaker, A.W.5
Martin, R.H.6
-
98
-
-
0027537281
-
Chromosome analysis of human spermatozoa stored in vitro
-
Munné S, Estop AM (1993) Chromosome analysis of human spermatozoa stored in vitro. Hum Reprod 8 : 581-586
-
(1993)
Hum Reprod
, vol.8
, pp. 581-586
-
-
Munné, S.1
Estop, A.M.2
-
99
-
-
0027489620
-
Segregation analysis in a man heterozygous for a pericentric inversion of chromosome 7(p13;q36) by sperm chromosome studies
-
Navarro J, Benet J, Martorell MR, Templado C, Egozcue J (1993) Segregation analysis in a man heterozygous for a pericentric inversion of chromosome 7(p13;q36) by sperm chromosome studies. Am J Hum Genet 53 : 214-219
-
(1993)
Am J Hum Genet
, vol.53
, pp. 214-219
-
-
Navarro, J.1
Benet, J.2
Martorell, M.R.3
Templado, C.4
Egozcue, J.5
-
100
-
-
0025921769
-
Chromosome abnormalities found among 34910 newborn children: Results from a 13-year incidence study in Århus, Denmark
-
Nielsen J, Wohlert M (1991) Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in Århus, Denmark. Hum Genet 87 : 81-83
-
(1991)
Hum Genet
, vol.87
, pp. 81-83
-
-
Nielsen, J.1
Wohlert, M.2
-
101
-
-
0019969295
-
Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969-1974 and 1980-1982 in the same area
-
Nielsen J, Wohlert M, Faaborg-Andersen J, Hansen KB, Hvidman L, Krag-Olsen B, Moulvad I, Videbech P (1982) Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969-1974 and 1980-1982 in the same area. Hum Genet 61 : 98-101
-
(1982)
Hum Genet
, vol.61
, pp. 98-101
-
-
Nielsen, J.1
Wohlert, M.2
Faaborg-Andersen, J.3
Hansen, K.B.4
Hvidman, L.5
Krag-Olsen, B.6
Moulvad, I.7
Videbech, P.8
-
102
-
-
0002087696
-
Preferential paternal origin of de novo structural chromosome rearrangements
-
Daniel A (ed) Liss, New York
-
Olson SB, Magenis RE (1988) Preferential paternal origin of de novo structural chromosome rearrangements. In: Daniel A (ed) The cytogenetics of mammalian autosomal rearrangements. Liss, New York, pp 583-599
-
(1988)
The Cytogenetics of Mammalian Autosomal Rearrangements
, pp. 583-599
-
-
Olson, S.B.1
Magenis, R.E.2
-
103
-
-
0342761339
-
Aneuploidy detection for chromosomes 1, X and Y by fluorescence in situ hybridization in human sperm from oligoasthenoteratozoospermic patients
-
Pang MG, Zackowski JL, Ryu BY, Moon SY, Acosta AA, Kearns WG (1994) Aneuploidy detection for chromosomes 1, X and Y by fluorescence in situ hybridization in human sperm from oligoasthenoteratozoospermic patients. Am J Hum Genet 55 : A113
-
(1994)
Am J Hum Genet
, vol.55
-
-
Pang, M.G.1
Zackowski, J.L.2
Ryu, B.Y.3
Moon, S.Y.4
Acosta, A.A.5
Kearns, W.G.6
-
104
-
-
0015443112
-
Chromosomal aneuploidy in human spermatozoa
-
Pawlowitzki IH, Pearson PL (1972) Chromosomal aneuploidy in human spermatozoa. Hum Genet 16 : 119-122
-
(1972)
Hum Genet
, vol.16
, pp. 119-122
-
-
Pawlowitzki, I.H.1
Pearson, P.L.2
-
105
-
-
0014800091
-
Fluorescent staining of the Y chromosome in meiotic stages of the human male
-
Pearson PL, Bobrow M (1970) Fluorescent staining of the Y chromosome in meiotic stages of the human male. J Reprod Fertil 22 : 177-179
-
(1970)
J Reprod Fertil
, vol.22
, pp. 177-179
-
-
Pearson, P.L.1
Bobrow, M.2
-
106
-
-
0014932086
-
Technique for identifying Y chromosomes in human interphase nuclei
-
Pearson PL, Bobrow M, Vosa CG (1970) Technique for identifying Y chromosomes in human interphase nuclei. Nature 226 : 78-80
-
(1970)
Nature
, vol.226
, pp. 78-80
-
-
Pearson, P.L.1
Bobrow, M.2
Vosa, C.G.3
-
107
-
-
0025363466
-
Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature
-
Pellestor F (1990) Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature. Hum Genet 85 : 49-54
-
(1990)
Hum Genet
, vol.85
, pp. 49-54
-
-
Pellestor, F.1
-
108
-
-
0025938351
-
Differential distribution of aneuploidy in human gametes according to their sex
-
Pellestor F (1991) Differential distribution of aneuploidy in human gametes according to their sex. Hum Reprod 6 : 1252-1258
-
(1991)
Hum Reprod
, vol.6
, pp. 1252-1258
-
-
Pellestor, F.1
-
109
-
-
0023351609
-
Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation
-
Pellestor F, Sele B, Jalbert H (1987) Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation. Hum Genet 76 : 116-120
-
(1987)
Hum Genet
, vol.76
, pp. 116-120
-
-
Pellestor, F.1
Sele, B.2
Jalbert, H.3
-
110
-
-
0024589666
-
Direct segregation analysis of reciprocal translocations: A study of 283 sperm karyotypes from four carriers
-
Pellestor F, Sele B, Jalbert H, Jalbert P (1989) Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers. Am J Hum Genet 44 : 464-473
-
(1989)
Am J Hum Genet
, vol.44
, pp. 464-473
-
-
Pellestor, F.1
Sele, B.2
Jalbert, H.3
Jalbert, P.4
-
111
-
-
0030067902
-
Direct detection of disomy in human sperm by the PRINS technique
-
Pellestor F, Quennesson I, Coignet L, Girardet A, Andréo B, Charlieu JP (1996a) Direct detection of disomy in human sperm by the PRINS technique. Hum Genet 97 : 21-25
-
(1996)
Hum Genet
, vol.97
, pp. 21-25
-
-
Pellestor, F.1
Quennesson, I.2
Coignet, L.3
Girardet, A.4
Andréo, B.5
Charlieu, J.P.6
-
112
-
-
0029963127
-
Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using primed in situ labeling technique
-
Pellestor F, Girardet A, Coignet L, Andréo B, Charlieu JP (1996b) Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using primed in situ labeling technique. Am J Hum Genet 58 : 797-802
-
(1996)
Am J Hum Genet
, vol.58
, pp. 797-802
-
-
Pellestor, F.1
Girardet, A.2
Coignet, L.3
Andréo, B.4
Charlieu, J.P.5
-
113
-
-
0025306430
-
Human gametes and zygotes studied by nonradioactive in situ hybridization
-
Pieters MHEC, Geraedts JPM, Meyer H, Dumoulin JCM, Evers JLH, Jongbloed RJE, Nederlof PM, Flier S van der (1990) Human gametes and zygotes studied by nonradioactive in situ hybridization. Cytogenet Cell Genet 53 : 15-19
-
(1990)
Cytogenet Cell Genet
, vol.53
, pp. 15-19
-
-
Pieters, M.H.E.C.1
Geraedts, J.P.M.2
Meyer, H.3
Dumoulin, J.C.M.4
Evers, J.L.H.5
Jongbloed, R.J.E.6
Nederlof, P.M.7
Van Der, F.S.8
-
114
-
-
0027486737
-
Detection of aneuploid human sperm by fluorescence in situ hybridization: Evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y
-
Robbins WA, Segraves R, Pinkel D, Wyrobek AJ (1993) Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y. Am J Hum Genet 52 : 799-807
-
(1993)
Am J Hum Genet
, vol.52
, pp. 799-807
-
-
Robbins, W.A.1
Segraves, R.2
Pinkel, D.3
Wyrobek, A.J.4
-
115
-
-
0017121624
-
Y chromosome visibility in quinacrine-stained human spermatozoa
-
Roberts AM, Goodall H (1976) Y chromosome visibility in quinacrine-stained human spermatozoa. Nature 262 : 493-494
-
(1976)
Nature
, vol.262
, pp. 493-494
-
-
Roberts, A.M.1
Goodall, H.2
-
116
-
-
0030047175
-
Molecular studies of translocations and trisomy involving chromosome 13
-
Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA (1996) Molecular studies of translocations and trisomy involving chromosome 13. Am J Med Genet 61 : 158-163
-
(1996)
Am J Med Genet
, vol.61
, pp. 158-163
-
-
Robinson, W.P.1
Bernasconi, F.2
Dutly, F.3
Lefort, G.4
Romain, D.R.5
Binkert, F.6
Schinzel, A.A.7
-
117
-
-
0025781920
-
Sperm chromosomes and habitual abortion
-
Rosenbusch B, Sterzik K (1991) Sperm chromosomes and habitual abortion. Fertil Steril 56 : 370-372
-
(1991)
Fertil Steril
, vol.56
, pp. 370-372
-
-
Rosenbusch, B.1
Sterzik, K.2
-
118
-
-
0025782823
-
Zytogenetische Analyse der Spermienchromosomen bei Paaren mit habituellen Aborten
-
Rosenbusch B, Sterzik K, Lauritzen C (1991) Zytogenetische Analyse der Spermienchromosomen bei Paaren mit habituellen Aborten. Geburtshilfe Frauenheilkd 51 : 369-372
-
(1991)
Geburtshilfe Frauenheilkd
, vol.51
, pp. 369-372
-
-
Rosenbusch, B.1
Sterzik, K.2
Lauritzen, C.3
-
119
-
-
0026460135
-
Cytogenetics of human spermatozoa: Correlations with sperm morphology and age of fertile men
-
Rosenbusch B, Strehler E, Sterzik K (1992) Cytogenetics of human spermatozoa: correlations with sperm morphology and age of fertile men. Fertil Steril 58 : 1071-1072
-
(1992)
Fertil Steril
, vol.58
, pp. 1071-1072
-
-
Rosenbusch, B.1
Strehler, E.2
Sterzik, K.3
-
120
-
-
0027514136
-
Die Korrelation zwischen zytogenetischen Anomalien menschlicher Spermatozoen und der Spermienmorphologie sowie dem Alter der untersuchten Personen
-
Rosenbusch B, Strehler E, Abt M, Sterzik K (1993) Die Korrelation zwischen zytogenetischen Anomalien menschlicher Spermatozoen und der Spermienmorphologie sowie dem Alter der untersuchten Personen. Zentralbl Gynakol 115 : 113-116
-
(1993)
Zentralbl Gynakol
, vol.115
, pp. 113-116
-
-
Rosenbusch, B.1
Strehler, E.2
Abt, M.3
Sterzik, K.4
-
121
-
-
0021985318
-
Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human sterility
-
Rosenmann A, Wahrman J, Richler C, Voss R, Persitz A, Goldman B (1985) Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human sterility. Cytogenet Cell Genet 39 : 19-29
-
(1985)
Cytogenet Cell Genet
, vol.39
, pp. 19-29
-
-
Rosenmann, A.1
Wahrman, J.2
Richler, C.3
Voss, R.4
Persitz, A.5
Goldman, B.6
-
122
-
-
0029050243
-
In-vitro decondensation of human spermatozoa for fluorescence in-situ hybridization
-
Rousseaux S, Chevret E (1995) In-vitro decondensation of human spermatozoa for fluorescence in-situ hybridization. Hum Reprod 10 : 2209-2213
-
(1995)
Hum Reprod
, vol.10
, pp. 2209-2213
-
-
Rousseaux, S.1
Chevret, E.2
-
123
-
-
0028841197
-
Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes
-
Rousseaux S, Chevret E, Monteil M, Cozzi J, Pelletier R, Delafontaine D, Sèle B (1995a) Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes. Hum Genet 96 : 655-660
-
(1995)
Hum Genet
, vol.96
, pp. 655-660
-
-
Rousseaux, S.1
Chevret, E.2
Monteil, M.3
Cozzi, J.4
Pelletier, R.5
Delafontaine, D.6
Sèle, B.7
-
124
-
-
0028869099
-
Meiotic segregation in males heterozygote for reciprocal translocations: Analysis of sperm nuclei by two and three colour fluorescence in situ hybridization
-
Rousseaux S, Chevret E, Monteil M, Cozzi J, Pelletier R, Devillard F, Lespinasse J, Sèle B (1995b) Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization. Cytogenet Cell Genet 71 : 240-246
-
(1995)
Cytogenet Cell Genet
, vol.71
, pp. 240-246
-
-
Rousseaux, S.1
Chevret, E.2
Monteil, M.3
Cozzi, J.4
Pelletier, R.5
Devillard, F.6
Lespinasse, J.7
Sèle, B.8
-
125
-
-
0018080015
-
Direct analysis of the chromosome constitution of human spermatozoa
-
Rudak E, Jacobs PA, Yanagimachi R (1978) Direct analysis of the chromosome constitution of human spermatozoa. Nature 274 : 911-913
-
(1978)
Nature
, vol.274
, pp. 911-913
-
-
Rudak, E.1
Jacobs, P.A.2
Yanagimachi, R.3
-
126
-
-
0027818575
-
Aneuploidy in spermatozoa using fluorescence in situ hybridization
-
Schattman GL, Munné S, Grifo JG, Carton L, Cohen J (1993) Aneuploidy in spermatozoa using fluorescence in situ hybridization. J Assist Reprod Genet 10 : 360-365
-
(1993)
J Assist Reprod Genet
, vol.10
, pp. 360-365
-
-
Schattman, G.L.1
Munné, S.2
Grifo, J.G.3
Carton, L.4
Cohen, J.5
-
127
-
-
0026599790
-
Sperm chromosome complements from two human reciprocal translocation heterozygotes
-
Spriggs EL, Martin RH, Hultén M (1992) Sperm chromosome complements from two human reciprocal translocation heterozygotes. Hum Genet 88 : 447-452
-
(1992)
Hum Genet
, vol.88
, pp. 447-452
-
-
Spriggs, E.L.1
Martin, R.H.2
Hultén, M.3
-
128
-
-
0029016039
-
Aneuploidy in human sperm: Results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y
-
Spriggs EL, Rademaker AW, Martin RH (1995) Aneuploidy in human sperm: results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y. Cytogenet Cell Genet 71 : 47-53
-
(1995)
Cytogenet Cell Genet
, vol.71
, pp. 47-53
-
-
Spriggs, E.L.1
Rademaker, A.W.2
Martin, R.H.3
-
129
-
-
0030052506
-
Aneuploidy in human sperm: The use of multicolor FISH to test various theories of nondisjunction
-
Spriggs EL, Rademaker AW, Martin RH (1996) Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction. Am J Hum Genet 58 : 356-362
-
(1996)
Am J Hum Genet
, vol.58
, pp. 356-362
-
-
Spriggs, E.L.1
Rademaker, A.W.2
Martin, R.H.3
-
130
-
-
0026766967
-
Meiotic segregation of a 21;22 Robertsonian translocation
-
Syme RM, Martin RH (1992) Meiotic segregation of a 21;22 Robertsonian translocation. Hum Reprod 7 : 825-829
-
(1992)
Hum Reprod
, vol.7
, pp. 825-829
-
-
Syme, R.M.1
Martin, R.H.2
-
131
-
-
0000330352
-
An air-drying method for chromosome preparation from mouse eggs
-
Tarkowski AK (1966) An air-drying method for chromosome preparation from mouse eggs. Cytogenetics 5 : 394-400
-
(1966)
Cytogenetics
, vol.5
, pp. 394-400
-
-
Tarkowski, A.K.1
-
132
-
-
0021238541
-
Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation
-
Templado C, Vidal F, Navarro J, Marina S, Egozcue J (1984) Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation. Hum Genet 67 : 162-165
-
(1984)
Hum Genet
, vol.67
, pp. 162-165
-
-
Templado, C.1
Vidal, F.2
Navarro, J.3
Marina, S.4
Egozcue, J.5
-
133
-
-
0023854130
-
Human sperm chromosomes
-
Templado C, Benet J, Genescà A, Navarro J, Caballin MR, Miro R, Egozcue J (1988a) Human sperm chromosomes. Hum Reprod 3 : 133-138
-
(1988)
Hum Reprod
, vol.3
, pp. 133-138
-
-
Templado, C.1
Benet, J.2
Genescà, A.3
Navarro, J.4
Caballin, M.R.5
Miro, R.6
Egozcue, J.7
-
134
-
-
0023908684
-
Human sperm chromosome studies in a reciprocal translocation t(2;5)
-
Templado C, Navarro J, Benet J, Genescà A, Pérez MM, Egozcue J (1988b) Human sperm chromosome studies in a reciprocal translocation t(2;5). Hum Genet 79 : 24-28
-
(1988)
Hum Genet
, vol.79
, pp. 24-28
-
-
Templado, C.1
Navarro, J.2
Benet, J.3
Genescà, A.4
Pérez, M.M.5
Egozcue, J.6
-
135
-
-
0025129345
-
Meiotic and sperm chromosome studies in a reciprocal translocation, t(1;2)(q32;q36)
-
Templado C, Navarro J, Requena R, Benet J, Ballesta F, Egozcue J (1990) Meiotic and sperm chromosome studies in a reciprocal translocation, t(1;2)(q32;q36). Hum Genet 84 : 159-162
-
(1990)
Hum Genet
, vol.84
, pp. 159-162
-
-
Templado, C.1
Navarro, J.2
Requena, R.3
Benet, J.4
Ballesta, F.5
Egozcue, J.6
-
136
-
-
10544240761
-
An analysis of human sperm chromosome aneuploidy
-
Templado C, Márquez C, Munné S, Colls P, Martorell MR, Cieply K, Benet J, Van Kirk V, Navarro J, Estop AM (1996) An analysis of human sperm chromosome aneuploidy. Cytogenet Cell Genet 74 : 194-200
-
(1996)
Cytogenet Cell Genet
, vol.74
, pp. 194-200
-
-
Templado, C.1
Márquez, C.2
Munné, S.3
Colls, P.4
Martorell, M.R.5
Cieply, K.6
Benet, J.7
Van Kirk, V.8
Navarro, J.9
Estop, A.M.10
-
137
-
-
0029833814
-
Simultaneous detection of structural and numerical chromosome abnormalities in sperm of healthy men by multicolor fluorescence in situ hybridization
-
Van Hummelen P, Lowe XR, Wyrobek AJ (1996) Simultaneous detection of structural and numerical chromosome abnormalities in sperm of healthy men by multicolor fluorescence in situ hybridization. Hum Genet 98 : 608-615
-
(1996)
Hum Genet
, vol.98
, pp. 608-615
-
-
Van Hummelen, P.1
Lowe, X.R.2
Wyrobek, A.J.3
-
138
-
-
0020062543
-
Meiotic and synaptonemal complex studies in a 14/21 translocation carrier
-
Vidal F, Templado C, Navarro J, Marina S, Egozcue J (1982) Meiotic and synaptonemal complex studies in a 14/21 translocation carrier. Int J Androl 5 : 21-26
-
(1982)
Int J Androl
, vol.5
, pp. 21-26
-
-
Vidal, F.1
Templado, C.2
Navarro, J.3
Marina, S.4
Egozcue, J.5
-
139
-
-
0023104262
-
Trisomy 1 in an eight cell human preembryo
-
Watt JL, Templeton AA, Messinis I, Bell L, Cunningham P, Duncan RO (1987) Trisomy 1 in an eight cell human preembryo. J Med Genet 24 : 60-64
-
(1987)
J Med Genet
, vol.24
, pp. 60-64
-
-
Watt, J.L.1
Templeton, A.A.2
Messinis, I.3
Bell, L.4
Cunningham, P.5
Duncan, R.O.6
-
140
-
-
0027372861
-
Non-disjunction in human sperm: Results of fluorescence in situ hybridization studies using two and three probes
-
Williams BJ, Ballenger CA, Malter HE, Bishop F, Tucker M, Zwingman TA, Tassold TJ (1993) Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Hum Mol Genet 2 : 1929-1936
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1929-1936
-
-
Williams, B.J.1
Ballenger, C.A.2
Malter, H.E.3
Bishop, F.4
Tucker, M.5
Zwingman, T.A.6
Tassold, T.J.7
-
141
-
-
0343307102
-
Detection of human sperm carrying sex chromosomal and autosomal aneuploidies using one, two, and three-color fluorescence in situ hybridizations
-
Wyrobek AJ, Robbins WA, Weier H-U, Pinkel D (1992) Detection of human sperm carrying sex chromosomal and autosomal aneuploidies using one, two, and three-color fluorescence in situ hybridizations. Am J Hum Genet 51 : A23
-
(1992)
Am J Hum Genet
, vol.51
-
-
Wyrobek, A.J.1
Robbins, W.A.2
Weier, H.-U.3
Pinkel, D.4
-
142
-
-
0028029824
-
Detection of sex chromosomal aneuploidies X-X, Y-Y, and X-Y in human sperm using two chromosome fluorescence in situ hybridization
-
Wyrobek AJ, Robbins WA, Mehraein Y, Pinkel D, Weier H-U (1994) Detection of sex chromosomal aneuploidies X-X, Y-Y, and X-Y in human sperm using two chromosome fluorescence in situ hybridization. Am J Med Genet 53 : 1-7
-
(1994)
Am J Med Genet
, vol.53
, pp. 1-7
-
-
Wyrobek, A.J.1
Robbins, W.A.2
Mehraein, Y.3
Pinkel, D.4
Weier, H.-U.5
-
143
-
-
0011018090
-
Investigation of metaphase chromosomes with DNA-binding fluorochromes
-
Zech L (1969) Investigation of metaphase chromosomes with DNA-binding fluorochromes. Exp Cell Res 58 : 463
-
(1969)
Exp Cell Res
, vol.58
, pp. 463
-
-
Zech, L.1
|