-
1
-
-
0032918559
-
Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein
-
Anderson LK, Reeves A, Webb LM, Ashley T: Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein. Genetics 151:1569-1579 (1999).
-
(1999)
Genetics
, vol.151
, pp. 1569-1579
-
-
Anderson, L.K.1
Reeves, A.2
Webb, L.M.3
Ashley, T.4
-
2
-
-
0033214543
-
Screening for abnormalities of chromosomes X, Y, and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program
-
Aran B, Blanco J, Vidal F, Vendrell J, Egozcue S, Barri P, Egozcue J, Veiga A: Screening for abnormalities of chromosomes X, Y, and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program. Fertil Steril 72:696-701 (1999).
-
(1999)
Fertil Steril
, vol.72
, pp. 696-701
-
-
Aran, B.1
Blanco, J.2
Vidal, F.3
Vendrell, J.4
Egozcue, S.5
Barri, P.6
Egozcue, J.7
Veiga, A.8
-
3
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, Yao X, et al: Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat Genet 13:336-342 (1996).
-
(1996)
Nat Genet
, vol.13
, pp. 336-342
-
-
Baker, S.M.1
Plug, A.W.2
Prolla, T.A.3
Bronner, C.E.4
Harris, A.C.5
Yao, X.6
-
4
-
-
0031829611
-
Crossing over analysis at pachytene in man
-
Barlow AL, Hultén MA: Crossing over analysis at pachytene in man. Eur J Hum Genet 6:350-358 (1998).
-
(1998)
Eur J Hum Genet
, vol.6
, pp. 350-358
-
-
Barlow, A.L.1
Hultén, M.A.2
-
5
-
-
0032407968
-
Case report: Paternal origin of trisomy 21 following intracytoplasmic sperm injection (ICSI)
-
Bartels I, Schlosser M, Bartz U, Pauer H: Case report: paternal origin of trisomy 21 following intracytoplasmic sperm injection (ICSI). Hum Reprod 13:3345-3346 (1998).
-
(1998)
Hum Reprod
, vol.13
, pp. 3345-3346
-
-
Bartels, I.1
Schlosser, M.2
Bartz, U.3
Pauer, H.4
-
6
-
-
0032231320
-
Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: Increased incidence in cases of paternal origin
-
Blanco J, Gabau E, Gomez D, Baena N, Guitart M, Egozcue J, Vidal F: Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin. Am J Hum Genet 63:1067-1072 (1998).
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1067-1072
-
-
Blanco, J.1
Gabau, E.2
Gomez, D.3
Baena, N.4
Guitart, M.5
Egozcue, J.6
Vidal, F.7
-
7
-
-
0031811730
-
Incidence of chromosomal aberrations in children born after assisted reproduction through intracytoplasmic sperm injections
-
Bonduelle M, Aytoz A, Van Assche E, Devroey P, Liebaers I, Van Steirteghem A: Incidence of chromosomal aberrations in children born after assisted reproduction through intracytoplasmic sperm injections. Hum Reprod 13:781-782 (1998).
-
(1998)
Hum Reprod
, vol.13
, pp. 781-782
-
-
Bonduelle, M.1
Aytoz, A.2
Van Assche, E.3
Devroey, P.4
Liebaers, I.5
Van Steirteghem, A.6
-
8
-
-
0021908105
-
Chromosomes of human sperm: Variability among normal individuals
-
Brandriff B, Gordon L, Ashworth L, Watchmaker G, Moore I, Wyrobek A, Carrano A: Chromosomes of human sperm: variability among normal individuals. Hum Genet 70:18-24 (1985).
-
(1985)
Hum Genet
, vol.70
, pp. 18-24
-
-
Brandriff, B.1
Gordon, L.2
Ashworth, L.3
Watchmaker, G.4
Moore, I.5
Wyrobek, A.6
Carrano, A.7
-
9
-
-
9444239304
-
Defective recombination in infertile men
-
Gonsalves J, Sun F, Schlegel PN, Turek PJ, Hopps CV, Greene C, Martin RH, Reijo Pera RA: Defective recombination in infertile men. Hum Mol Genet 13:2875-2883 (2004).
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2875-2883
-
-
Gonsalves, J.1
Sun, F.2
Schlegel, P.N.3
Turek, P.J.4
Hopps, C.V.5
Greene, C.6
Martin, R.H.7
Reijo Pera, R.A.8
-
10
-
-
0035319804
-
To err (meiotically) is human: The genesis of human aneuploidy
-
Hassold T, Hunt P: To err (meiotically) is human: the genesis of human aneuploidy. Nat Rev Genet 2:280-291 (2001).
-
(2001)
Nat Rev Genet
, vol.2
, pp. 280-291
-
-
Hassold, T.1
Hunt, P.2
-
11
-
-
0026334334
-
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
-
Hassold T, Sherman S, Pettay D, Page D, Jacobs P: XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet 49:253-260 (1991).
-
(1991)
Am J Hum Genet
, vol.49
, pp. 253-260
-
-
Hassold, T.1
Sherman, S.2
Pettay, D.3
Page, D.4
Jacobs, P.5
-
12
-
-
0029818072
-
Human aneuploidy: Incidence, origin, and etiology
-
Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M, Millie E, et al: Human aneuploidy: incidence, origin, and etiology. Environ Mol Mutagen 28:167-175 (1996).
-
(1996)
Environ Mol Mutagen
, vol.28
, pp. 167-175
-
-
Hassold, T.1
Abruzzo, M.2
Adkins, K.3
Griffin, D.4
Merrill, M.5
Millie, E.6
-
13
-
-
0035988228
-
Chromosome abnormalities in sperm from infertile men with asthenoteratozoospermia
-
Hristova R, Ko E, Greene C, Rademaker A, Chernos J, Martin R: Chromosome abnormalities in sperm from infertile men with asthenoteratozoospermia. Biol Reprod 66:1781-1783 (2002).
-
(2002)
Biol Reprod
, vol.66
, pp. 1781-1783
-
-
Hristova, R.1
Ko, E.2
Greene, C.3
Rademaker, A.4
Chernos, J.5
Martin, R.6
-
14
-
-
0031698004
-
Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility: Recommendations for genetic counseling and screening
-
Johnson M: Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility: recommendations for genetic counseling and screening. Fertil Steril 70:397-411 (1998).
-
(1998)
Fertil Steril
, vol.70
, pp. 397-411
-
-
Johnson, M.1
-
15
-
-
0347356254
-
Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex
-
Judis L, Chan ER, Schwartz S, Seftel A, Hassold T: Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex. Fertil Steril 81:205-209 (2004).
-
(2004)
Fertil Steril
, vol.81
, pp. 205-209
-
-
Judis, L.1
Chan, E.R.2
Schwartz, S.3
Seftel, A.4
Hassold, T.5
-
16
-
-
0009475717
-
Fluorescence in situ hybridization (FISH) analysis in sperm cells
-
Wegner R (ed): Springer, Berlin
-
Ko E, Martin R: Fluorescence in situ hybridization (FISH) analysis in sperm cells, in Wegner R (ed): Diagnostic Genetics, pp 335-355 (Springer, Berlin 1999).
-
(1999)
Diagnostic Genetics
, pp. 335-355
-
-
Ko, E.1
Martin, R.2
-
17
-
-
0036278943
-
Microwave decondensation and codenaturation: A new methodology to maximize FISH data from donors with very low concentrations of sperm
-
Ko E, Rademaker A, Martin R: Microwave decondensation and codenaturation: a new methodology to maximize FISH data from donors with very low concentrations of sperm. Cytogenet Cell Genet 95:143-145 (2001).
-
(2001)
Cytogenet Cell Genet
, vol.95
, pp. 143-145
-
-
Ko, E.1
Rademaker, A.2
Martin, R.3
-
19
-
-
0026705388
-
Reduced recombination and paternal age effect in Klinefelter syndrome
-
Lorda-Sanchez I, Binkert F, Maechler M, Robinson WP, Schinzel AA: Reduced recombination and paternal age effect in Klinefelter syndrome. Hum Genet 89:524-530 (1992).
-
(1992)
Hum Genet
, vol.89
, pp. 524-530
-
-
Lorda-Sanchez, I.1
Binkert, F.2
Maechler, M.3
Robinson, W.P.4
Schinzel, A.A.5
-
20
-
-
0037150706
-
Covariation of synaptonemal complex length and mammalian meiotic exchange rates
-
Lynn A, Koehler KE, Judis L, Chan ER, Cherry JP, Schwartz S, et al: Covariation of synaptonemal complex length and mammalian meiotic exchange rates. Science 296:2222-2225 (2002).
-
(2002)
Science
, vol.296
, pp. 2222-2225
-
-
Lynn, A.1
Koehler, K.E.2
Judis, L.3
Chan, E.R.4
Cherry, J.P.5
Schwartz, S.6
-
21
-
-
0028030585
-
The origin of 47,XXY and 47,XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination
-
MacDonald M, Hassold T, Harvey J, Wang L, Morton N, Jacobs P: The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination. Hum Mol Genet 3:1365-1371 (1994).
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1365-1371
-
-
MacDonald, M.1
Hassold, T.2
Harvey, J.3
Wang, L.4
Morton, N.5
Jacobs, P.6
-
22
-
-
0033868950
-
Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro
-
Magli MC, Jones GM, Gras L, Gianaroli L, Korman I, Trounson AO: Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro. Hum Reprod 15:1781-1786 (2000).
-
(2000)
Hum Reprod
, vol.15
, pp. 1781-1786
-
-
Magli, M.C.1
Jones, G.M.2
Gras, L.3
Gianaroli, L.4
Korman, I.5
Trounson, A.O.6
-
23
-
-
0029886954
-
The risk of chromosomal abnormalities following ICSI
-
Martin R: The risk of chromosomal abnormalities following ICSI. Hum Reprod 11:924-925 (1996).
-
(1996)
Hum Reprod
, vol.11
, pp. 924-925
-
-
Martin, R.1
-
24
-
-
0029134776
-
Reliability of aneuploidy estimates in human sperm: Results of fluorescence in situ hybridization studies using two different scoring criteria
-
Martin R, Rademaker A: 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).
-
(1995)
Mol Reprod Dev
, vol.42
, pp. 89-93
-
-
Martin, R.1
Rademaker, A.2
-
25
-
-
0020051046
-
Direct chromosomal analysis of human spermatozoa: Preliminary results from 18 normal men
-
Martin R, Lin C, Balkan W, Burns K: Direct chromosomal analysis of human spermatozoa: preliminary results from 18 normal men. Am J Hum Genet 34:459-468 (1982).
-
(1982)
Am J Hum Genet
, vol.34
, pp. 459-468
-
-
Martin, R.1
Lin, C.2
Balkan, W.3
Burns, K.4
-
26
-
-
0020608012
-
The chromosome constitution of 1000 human spermatozoa
-
Martin R, Balkan W, Burns K, Rademaker A, Lin C, Rudd N: The chromosome constitution of 1000 human spermatozoa. Hum Genet 63:305-309 (1983).
-
(1983)
Hum Genet
, vol.63
, pp. 305-309
-
-
Martin, R.1
Balkan, W.2
Burns, K.3
Rademaker, A.4
Lin, C.5
Rudd, N.6
-
27
-
-
0025853757
-
Distribution of aneuploidy in human gametes: Comparison between human sperm and oocytes
-
Martin R, Ko E, Rademaker A: Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes. Am J Med Genet 39:321-331 (1991).
-
(1991)
Am J Med Genet
, vol.39
, pp. 321-331
-
-
Martin, R.1
Ko, E.2
Rademaker, A.3
-
28
-
-
0342832648
-
Human sperm karyotypes
-
Verma RS, Babu A (eds): McGraw-Hill, New York
-
Martin R, Ko E, Barclay L: Human sperm karyotypes, in Verma RS, Babu A (eds): Human Chromosomes: Manual of Basic Techniques, pp 56-65 (McGraw-Hill, New York 1994).
-
(1994)
Human Chromosomes: Manual of Basic Techniques
, pp. 56-65
-
-
Martin, R.1
Ko, E.2
Barclay, L.3
-
29
-
-
0033555701
-
Analysis of sperm chromosome complements before, during, and after chemotherapy
-
Martin R, Ernst S, Rademaker A, Barclay L, Ko E, Summers N: Analysis of sperm chromosome complements before, during, and after chemotherapy. Cancer Genet Cytogenet 108:133-136 (1999).
-
(1999)
Cancer Genet Cytogenet
, vol.108
, pp. 133-136
-
-
Martin, R.1
Ernst, S.2
Rademaker, A.3
Barclay, L.4
Ko, E.5
Summers, N.6
-
30
-
-
0034100519
-
Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia
-
Martin R, Greene C, Rademaker A, Barclay L, Ko E, Chernos J: Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia. Hum Reprod 15:1121-1124 (2000).
-
(2000)
Hum Reprod
, vol.15
, pp. 1121-1124
-
-
Martin, R.1
Greene, C.2
Rademaker, A.3
Barclay, L.4
Ko, E.5
Chernos, J.6
-
31
-
-
2942589927
-
Analysis of aneuploidy in spermatozoa from testicular biopsies from men with nonobstructive azoospermia
-
Martin RH, Greene C, Rademaker A, Ko E, Chernos J: Analysis of aneuploidy in spermatozoa from testicular biopsies from men with nonobstructive azoospermia. J Androl 24:100-103 (2003a).
-
(2003)
J Androl
, vol.24
, pp. 100-103
-
-
Martin, R.H.1
Greene, C.2
Rademaker, A.3
Ko, E.4
Chernos, J.5
-
32
-
-
0038638197
-
A comparison of the frequency of sperm chromosome abnormalities in men with mild, moderate, and severe oligozoospermia
-
Martin RH, Rademaker AW, Greene C, Ko E, Hoang T, Barclay L, Chernos J: A comparison of the frequency of sperm chromosome abnormalities in men with mild, moderate, and severe oligozoospermia. Biol Reprod 69:535-539 (2003b).
-
(2003)
Biol Reprod
, vol.69
, pp. 535-539
-
-
Martin, R.H.1
Rademaker, A.W.2
Greene, C.3
Ko, E.4
Hoang, T.5
Barclay, L.6
Chernos, J.7
-
33
-
-
0031761587
-
Abnormalities for chromosomes 13 and 21 detected in spermatozoa from infertile men
-
McInnes B, Rademaker A, Greene C, Ko E, Barclay L, Martin R: Abnormalities for chromosomes 13 and 21 detected in spermatozoa from infertile men. Hum Reprod 13:2787-2790 (1998).
-
(1998)
Hum Reprod
, vol.13
, pp. 2787-2790
-
-
McInnes, B.1
Rademaker, A.2
Greene, C.3
Ko, E.4
Barclay, L.5
Martin, R.6
-
34
-
-
0024988728
-
Spontaneous and in vitro radiation-induced chromosome aberrations in human spermatozoa: Application of a new method
-
Mendelsohn ML, Albertini RJ (eds): John Wiley & Sons, Toronto
-
Mikamo K, Kamiguchi Y, Tateno H: Spontaneous and in vitro radiation-induced chromosome aberrations in human spermatozoa: Application of a new method, in Mendelsohn ML, Albertini RJ (eds): Mutation and the Environment, Part B: Metabolism, Testing Methods, and Chromosomes: Proceedings of the Fifth International Conference on Environmental Mutagens, pp 447-456 (John Wiley & Sons, Toronto 1990).
-
(1990)
Mutation and the Environment, Part B: Metabolism, Testing Methods, and Chromosomes: Proceedings of the Fifth International Conference on Environmental Mutagens
, pp. 447-456
-
-
Mikamo, K.1
Kamiguchi, Y.2
Tateno, H.3
-
35
-
-
0029087947
-
Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization
-
Moosani N, Pattinson H, Carter M, Cox D, Rademaker A, Martin R: Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization. Fertil Steril 64:811-817 (1995).
-
(1995)
Fertil Steril
, vol.64
, pp. 811-817
-
-
Moosani, N.1
Pattinson, H.2
Carter, M.3
Cox, D.4
Rademaker, A.5
Martin, R.6
-
36
-
-
0033995862
-
Sex chromosomal analysis of spermatozoa from infertile men using fluorescence in situ hybridization
-
Nishikawa N, Murakami I, Ikuta K, Suzumori K: Sex chromosomal analysis of spermatozoa from infertile men using fluorescence in situ hybridization. J Assist Reprod Genet 17:97-102 (2000).
-
(2000)
J Assist Reprod Genet
, vol.17
, pp. 97-102
-
-
Nishikawa, N.1
Murakami, I.2
Ikuta, K.3
Suzumori, K.4
-
37
-
-
0034967243
-
Meiotic segregation analysis in a t(4;8) carrier: Comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei
-
Oliver-Bonet M, Navarro J, Codina-Pascual M, Carrera M, Egozcue J, Benet J: Meiotic segregation analysis in a t(4;8) carrier: comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei. Eur J Hum Genet 9:395-403 (2001).
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 395-403
-
-
Oliver-Bonet, M.1
Navarro, J.2
Codina-Pascual, M.3
Carrera, M.4
Egozcue, J.5
Benet, J.6
-
38
-
-
0032905397
-
Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection
-
Pang M, Hoegerman S, Cuticchia A, Moon S, Doncel G, Acosta A, Kearns W: Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection. Hum Reprod 14:1266-1273 (1999).
-
(1999)
Hum Reprod
, vol.14
, pp. 1266-1273
-
-
Pang, M.1
Hoegerman, S.2
Cuticchia, A.3
Moon, S.4
Doncel, G.5
Acosta, A.6
Kearns, W.7
-
39
-
-
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, Andreo B, Charlieu J: 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).
-
(1996)
Am J Hum Genet
, vol.58
, pp. 797-802
-
-
Pellestor, F.1
Girardet, A.2
Coignet, L.3
Andreo, B.4
Charlieu, J.5
-
40
-
-
0018080015
-
Direct analysis of the chromosome constitution of human spermatozoa
-
Rudak E, Jacobs P, Yanagimachi R: Direct analysis of the chromosome constitution of human spermatozoa. Nature 274:911-913 (1978).
-
(1978)
Nature
, vol.274
, pp. 911-913
-
-
Rudak, E.1
Jacobs, P.2
Yanagimachi, R.3
-
41
-
-
0032512913
-
Aneuploidy and diploidy rates in sperm of five men after three-colour hybridization: Indication of X chromosome-associated autosome 2 aneuploidy
-
Scarpato R, Naccarati A, Mariani M, Migliore L: Aneuploidy and diploidy rates in sperm of five men after three-colour hybridization: indication of X chromosome-associated autosome 2 aneuploidy. Mutat Res 412:227-233 (1998).
-
(1998)
Mutat Res
, vol.412
, pp. 227-233
-
-
Scarpato, R.1
Naccarati, A.2
Mariani, M.3
Migliore, L.4
-
42
-
-
0033758969
-
Spontaneous frequencies of aneuploid and diploid sperm in 10 normal Chinese men: Assessed by multicolor fluorescence in situ hybridization
-
Shi Q, Martin R: Spontaneous frequencies of aneuploid and diploid sperm in 10 normal Chinese men: assessed by multicolor fluorescence in situ hybridization. Cytogenet Cell Genet 90:79-83 (2000).
-
(2000)
Cytogenet Cell Genet
, vol.90
, pp. 79-83
-
-
Shi, Q.1
Martin, R.2
-
43
-
-
0034998380
-
Aneuploidy in human spermatozoa: FISH analysis in men with constitutional chromosomal abnormalities, and in infertile men
-
Shi Q, Martin R: Aneuploidy in human spermatozoa: FISH analysis in men with constitutional chromosomal abnormalities, and in infertile men. Reproduction 121:655-666 (2001).
-
(2001)
Reproduction
, vol.121
, pp. 655-666
-
-
Shi, Q.1
Martin, R.2
-
44
-
-
0035865957
-
Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm
-
Shi Q, Spriggs E, Field L, Ko E, Barclay L, Martin R: Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm. Am J Med Genet 99:34-38 (2001).
-
(2001)
Am J Med Genet
, vol.99
, pp. 34-38
-
-
Shi, Q.1
Spriggs, E.2
Field, L.3
Ko, E.4
Barclay, L.5
Martin, R.6
-
45
-
-
0036077159
-
Absence of age effect on meiotic recombination between human X and Y chromosomes
-
Shi Q, Spriggs E, Field L, Rademaker A, Ko E, Barclay L, Martin R: Absence of age effect on meiotic recombination between human X and Y chromosomes. Am J Hum Genet 71:254-261 (2002).
-
(2002)
Am J Hum Genet
, vol.71
, pp. 254-261
-
-
Shi, Q.1
Spriggs, E.2
Field, L.3
Rademaker, A.4
Ko, E.5
Barclay, L.6
Martin, R.7
-
46
-
-
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 E, Rademaker A, Martin R: 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).
-
(1995)
Cytogenet Cell Genet
, vol.71
, pp. 47-53
-
-
Spriggs, E.1
Rademaker, A.2
Martin, R.3
-
47
-
-
0030052506
-
Aneuploidy in human sperm: The use of multicolor FISH to test various theories of nondisjunction
-
Spriggs E, Rademaker A, Martin R: Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction. Am J Hum Genet 58:356-362 (1996).
-
(1996)
Am J Hum Genet
, vol.58
, pp. 356-362
-
-
Spriggs, E.1
Rademaker, A.2
Martin, R.3
-
48
-
-
4344654289
-
Meiotic defects in a man with non-obstructive azoospermia: Case report
-
Sun F, Kozak G, Scott S, Trpkov K, Ko E, Mikhaail-Philips M, et al: Meiotic defects in a man with non-obstructive azoospermia: Case report. Hum Reprod 19:1770-1773 (2004a).
-
(2004)
Hum Reprod
, vol.19
, pp. 1770-1773
-
-
Sun, F.1
Kozak, G.2
Scott, S.3
Trpkov, K.4
Ko, E.5
Mikhaail-Philips, M.6
-
49
-
-
1542344378
-
Human male recombination maps for individual chromosomes
-
Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, et al: Human male recombination maps for individual chromosomes. Am J Hum Genet 74:521-531 (2004b).
-
(2004)
Am J Hum Genet
, vol.74
, pp. 521-531
-
-
Sun, F.1
Oliver-Bonet, M.2
Liehr, T.3
Starke, H.4
Ko, E.5
Rademaker, A.6
-
50
-
-
26244437300
-
Immunofluorescent synaptonemal complex analysis in azoospermic men
-
Sun F, Greene C, Turek PJ, Ko E, Rademaker A, Martin RH: Immunofluorescent synaptonemal complex analysis in azoospermic men. Cytogenet Genome Res 111:366-370 (2005).
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 366-370
-
-
Sun, F.1
Greene, C.2
Turek, P.J.3
Ko, E.4
Rademaker, A.5
Martin, R.H.6
-
51
-
-
0036091625
-
Patterns of meiotic recombination in human fetal oocytes
-
Tease C, Hartshorne GM, Hultén M: Patterns of meiotic recombination in human fetal oocytes. Am J Hum Genet 70:1469-1479 (2002).
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1469-1479
-
-
Tease, C.1
Hartshorne, G.M.2
Hultén, M.3
-
52
-
-
0036138671
-
Aneuploid spermatozoa in infertile men: Teratozoospermia
-
Templado C, Hoang T, Greene C, Rademaker A, Chernos J, Martin R: Aneuploid spermatozoa in infertile men: teratozoospermia. Mol Reprod Dev 61:200-204 (2002).
-
(2002)
Mol Reprod Dev
, vol.61
, pp. 200-204
-
-
Templado, C.1
Hoang, T.2
Greene, C.3
Rademaker, A.4
Chernos, J.5
Martin, R.6
-
53
-
-
0030918389
-
Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection
-
Van Opstal D, Los F, Ramlakhan S, Van Hemel J, Van Den Ouweland A, Brandenburg H, et al: Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection. Hum Reprod 12:682-686 (1997).
-
(1997)
Hum Reprod
, vol.12
, pp. 682-686
-
-
Van Opstal, D.1
Los, F.2
Ramlakhan, S.3
Van Hemel, J.4
Van Den Ouweland, A.5
Brandenburg, H.6
-
54
-
-
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, Hassold TJ: Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Hum Mol Genet 2:1929-1936 (1993).
-
(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
Hassold, T.J.7
-
55
-
-
0028029824
-
Detection of sex chromosomal aneuploidies X-X, Y-Y, and X-Y in human sperm using two-chromosome fluorescence in situ hybridization
-
Wyrobek A, Robbins W, Mehraein Y, Pinkel D, Weier H: 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).
-
(1994)
Am J Med Genet
, vol.53
, pp. 1-7
-
-
Wyrobek, A.1
Robbins, W.2
Mehraein, Y.3
Pinkel, D.4
Weier, H.5
-
56
-
-
0031791685
-
Studies of non-disjunction in trisomies 2, 7, 15, and 22: Does the parental origin of trisomy influence placental morphology?
-
Zaragoza MV, Millie E, Redline RW, Hassold TJ: Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? J Med Genet 35:924-931 (1998).
-
(1998)
J Med Genet
, vol.35
, pp. 924-931
-
-
Zaragoza, M.V.1
Millie, E.2
Redline, R.W.3
Hassold, T.J.4
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