-
1
-
-
0020608012
-
The chromosome constitution of 1000 human spermatozoa
-
Martin R, Balkan W, Burns K, et al.: The chromosome constitution of 1000 human spermatozoa. Hum Genet 1983;63:305-309
-
(1983)
Hum Genet
, vol.63
, pp. 305-309
-
-
Martin, R.1
Balkan, W.2
Burns, K.3
-
2
-
-
0023577485
-
The effect of age on the frequency of sperm chromosomal abnormalities in normal men
-
Martin R, Rademaker A: The effect of age on the frequency of sperm chromosomal abnormalities in normal men. Am J Hum Genet 1987;41:484-492
-
(1987)
Am J Hum Genet
, vol.41
, pp. 484-492
-
-
Martin, R.1
Rademaker, A.2
-
3
-
-
0023629482
-
Variation in the frequency and type of sperm chromosomal abnormalities among normal men
-
Martin R, Rademaker A, Hildebrand K, et al: Variation in the frequency and type of sperm chromosomal abnormalities among normal men. Hum Genet 1987;77:108-114
-
(1987)
Hum Genet
, vol.77
, pp. 108-114
-
-
Martin, R.1
Rademaker, A.2
Hildebrand, K.3
-
4
-
-
0023904370
-
The relationship between sperm chromosomal abnormalities and sperm morphology in humans
-
Martin R, Rademaker A: The relationship between sperm chromosomal abnormalities and sperm morphology in humans. Mutat Res 1988;207:159-164
-
(1988)
Mutat Res
, vol.207
, pp. 159-164
-
-
Martin, R.1
Rademaker, A.2
-
5
-
-
0024422670
-
A cytogenetic investigation of the effects of cryopreservation on human sperm
-
Chernos J, Martin R: A cytogenetic investigation of the effects of cryopreservation on human sperm. Am J Hum Genet 1989; 45:766-777
-
(1989)
Am J Hum Genet
, vol.45
, pp. 766-777
-
-
Chernos, J.1
Martin, R.2
-
6
-
-
0025331172
-
The frequency of aneuploidy for individual chromosomes in 6821 human sperm chromosome complements
-
Martin R, Rademaker A: The frequency of aneuploidy for individual chromosomes in 6821 human sperm chromosome complements. Cytogenet Cell Genet 1990;53:103-107
-
(1990)
Cytogenet Cell Genet
, vol.53
, pp. 103-107
-
-
Martin, R.1
Rademaker, A.2
-
7
-
-
0025853757
-
The distribution of aneuploidy in human gametes: Comparison between human sperm and oocytes
-
Martin R, Ko E, Rademaker A: The distribution of aneuploidy in human gametes: Comparison between human sperm and oocytes. Am J Med Genet 1991;39:321-331
-
(1991)
Am J Med Genet
, vol.39
, pp. 321-331
-
-
Martin, R.1
Ko, E.2
Rademaker, A.3
-
8
-
-
0025998091
-
The effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm
-
Martin R, Chernos J, Rademaker A: The effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm. Mol Reprod Dev 1991;30:159-163
-
(1991)
Mol Reprod Dev
, vol.30
, pp. 159-163
-
-
Martin, R.1
Chernos, J.2
Rademaker, A.3
-
9
-
-
0024653380
-
Invited Editorial: Segregation analysis of translocations by the study of human sperm chromosome complements
-
Martin R: Invited Editorial: Segregation analysis of translocations by the study of human sperm chromosome complements. Am J Hum Genet 1989;44:461-463
-
(1989)
Am J Hum Genet
, vol.44
, pp. 461-463
-
-
Martin, R.1
-
10
-
-
0026752917
-
Analysis of sperm chromosome complements from a man heterozygous for a Robertsonian translocation, 45,XY,t(15q22q)
-
Martin R, Ko E, Hildebrand K: Analysis of sperm chromosome complements from a man heterozygous for a Robertsonian translocation, 45,XY,t(15q22q). Am J Med Genet 1992;43: 855-857
-
(1992)
Am J Med Genet
, vol.43
, pp. 855-857
-
-
Martin, R.1
Ko, E.2
Hildebrand, K.3
-
11
-
-
0027399169
-
Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion, inv (8)(p23q22)
-
Martin R: Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion, inv (8)(p23q22). Cytogenet Cell Genet 1993;62:199-202
-
(1993)
Cytogenet Cell Genet
, vol.62
, pp. 199-202
-
-
Martin, R.1
-
12
-
-
0028118866
-
Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1
-
Martin R, Chernos J, Lowry R, et al.: Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1. Hum Genet 1994;93:135-138
-
(1994)
Hum Genet
, vol.93
, pp. 135-138
-
-
Martin, R.1
Chernos, J.2
Lowry, R.3
-
13
-
-
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 R, Spriggs E: 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 1995;47:42-46
-
(1995)
Clin Genet
, vol.47
, pp. 42-46
-
-
Martin, R.1
Spriggs, E.2
-
14
-
-
0013473677
-
A prospective serial study of the effects of radiotherapy on semen parameters, hamster egg penetration rates and lymphocyte chromosome abnormalities
-
Martin R, Rademaker A, Arthur K, et al.: A prospective serial study of the effects of radiotherapy on semen parameters, hamster egg penetration rates and lymphocyte chromosome abnormalities. Infertility 1985;8:97-112
-
(1985)
Infertility
, vol.8
, pp. 97-112
-
-
Martin, R.1
Rademaker, A.2
Arthur, K.3
-
15
-
-
0022902771
-
An increased frequency of human sperm chromosomal abnormalities after radiotherapy
-
Martin R, Hildebrand K, Yamamoto J, et al.: An increased frequency of human sperm chromosomal abnormalities after radiotherapy. Mutat Res 1986;174:219-225
-
(1986)
Mutat Res
, vol.174
, pp. 219-225
-
-
Martin, R.1
Hildebrand, K.2
Yamamoto, J.3
-
16
-
-
0024550835
-
A comparison of chromosomal aberrations induced by in vivo radiotherapy in human sperm and lymphocytes
-
Martin R, Rademaker A, Hildebrand K, et al.: A comparison of chromosomal aberrations induced by in vivo radiotherapy in human sperm and lymphocytes. Mutat Res 1989;226:21-30
-
(1989)
Mutat Res
, vol.226
, pp. 21-30
-
-
Martin, R.1
Rademaker, A.2
Hildebrand, K.3
-
17
-
-
0028958781
-
Analysis of chromosomal abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH)
-
Martin R, Rademaker A, Leonard N: Analysis of chromosomal abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH). Cancer Genet Cytogenet 1995;80:29-32
-
(1995)
Cancer Genet Cytogenet
, vol.80
, pp. 29-32
-
-
Martin, R.1
Rademaker, A.2
Leonard, N.3
-
18
-
-
0025077841
-
Fluorescence in situ hybridization to Y chromosomes in decondensed human sperm nuclei
-
Wyrobek A, Alhborn T, Balhorn R, et al.: Fluorescence in situ hybridization to Y chromosomes in decondensed human sperm nuclei. Mol Reprod Dev 1990;27:200-208
-
(1990)
Mol Reprod Dev
, vol.27
, pp. 200-208
-
-
Wyrobek, A.1
Alhborn, T.2
Balhorn, R.3
-
19
-
-
0025974026
-
Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa
-
Coonen E, Pieters M, Dumoulin J, et al: Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa. Mol Reprod Dev 1991;28:18-22
-
(1991)
Mol Reprod Dev
, vol.28
, pp. 18-22
-
-
Coonen, E.1
Pieters, M.2
Dumoulin, J.3
-
20
-
-
0025359715
-
Determination of Y chromosome aneuploidy in human sperm nuclei by non-radioactive in situ hybridization
-
Guttenbach M, Schmid M: Determination of Y chromosome aneuploidy in human sperm nuclei by non-radioactive in situ hybridization. Am J Hum Genet 1990;46:553-558
-
(1990)
Am J Hum Genet
, vol.46
, pp. 553-558
-
-
Guttenbach, M.1
Schmid, M.2
-
21
-
-
0025864454
-
Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei
-
Guttenbach M, Schmid M: Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei. Hum Genet 1991;87:261-265
-
(1991)
Hum Genet
, vol.87
, pp. 261-265
-
-
Guttenbach, M.1
Schmid, M.2
-
22
-
-
0026722597
-
Detection of chromosome 17- And X- bearing sperm in human spermatozoa using fluorescent in situ hybridization
-
Han T, Webb G, Flaherty S, et al.: Detection of chromosome 17- and X- bearing sperm in human spermatozoa using fluorescent in situ hybridization. Mol Reprod Dev 1992;33:189-194
-
(1992)
Mol Reprod Dev
, vol.33
, pp. 189-194
-
-
Han, T.1
Webb, G.2
Flaherty, S.3
-
23
-
-
0027516966
-
Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11)(p36.3;q13.1), using fluorescence in situ hybridisation
-
Goldman A, Hulten M: Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11)(p36.3;q13.1), using fluorescence in situ hybridisation. Cytogenet Cell Genet 1993;63:16-23
-
(1993)
Cytogenet Cell Genet
, vol.63
, pp. 16-23
-
-
Goldman, A.1
Hulten, M.2
-
24
-
-
0028055197
-
Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradiative in situ hybridization
-
Guttenbach M, Schakowski R, Schmid M: Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradiative in situ hybridization. Hum Genet 1994;93:7-12
-
(1994)
Hum Genet
, vol.93
, pp. 7-12
-
-
Guttenbach, M.1
Schakowski, R.2
Schmid, M.3
-
25
-
-
0028327204
-
Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization
-
Guttenbach M, Schakowski R, Schmid M: Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization. Hum Genet 1994;93:502-506
-
(1994)
Hum Genet
, vol.93
, pp. 502-506
-
-
Guttenbach, M.1
Schakowski, R.2
Schmid, M.3
-
26
-
-
0027456565
-
Simultaneous detection of X- And Y-bearing human sperm by double FISH
-
Han T, Ford J, Webb G, et al.: Simultaneous detection of X- and Y-bearing human sperm by double FISH. Mol Reprod Dev 1993;34:308-313
-
(1993)
Mol Reprod Dev
, vol.34
, pp. 308-313
-
-
Han, T.1
Ford, J.2
Webb, G.3
-
27
-
-
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 W, Segraves R, Pinkel D, et al.: 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 1993;52:799-807
-
(1993)
Am J Hum Genet
, vol.52
, pp. 799-807
-
-
Robbins, W.1
Segraves, R.2
Pinkel, D.3
-
28
-
-
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, et al.: 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 1994;53:1-7
-
(1994)
Am J Med Genet
, vol.53
, pp. 1-7
-
-
Wyrobek, A.1
Robbins, W.2
Mehraein, Y.3
-
29
-
-
0027406691
-
Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization
-
Holmes J, Martin R: Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization. Hum Genet 1993;91:20-24
-
(1993)
Hum Genet
, vol.91
, pp. 20-24
-
-
Holmes, J.1
Martin, R.2
-
30
-
-
0027363762
-
Detection of aneuploidy in human sperm by fluorescence in situ hybridization (FISH): Different frequencies in fresh and stored sperm nuclei
-
Martin R, Chan K, Ko E, et al.: Detection of aneuploidy in human sperm by fluorescence in situ hybridization (FISH): Different frequencies in fresh and stored sperm nuclei. Cytogenet Cell Genet 1994;65:95-96
-
(1994)
Cytogenet Cell Genet
, vol.65
, pp. 95-96
-
-
Martin, R.1
Chan, K.2
Ko, E.3
-
31
-
-
0028290235
-
Analysis of segregation in a human male reciprocal translocation carrier, t(1;11) (p36.3;q13.1), by two- Colour fluorescence in situ hybridization
-
Spriggs E, Martin R: Analysis of segregation in a human male reciprocal translocation carrier, t(1;11) (p36.3;q13.1), by two- colour fluorescence in situ hybridization. Mol Reprod Dev 1994;38:247-250
-
(1994)
Mol Reprod Dev
, vol.38
, pp. 247-250
-
-
Spriggs, E.1
Martin, R.2
-
32
-
-
0028212715
-
Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm
-
Bischoff F, Nguyen D, Burt K, et al.: Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenet Cell Genet 1994;66:237-243
-
(1994)
Cytogenet Cell Genet
, vol.66
, pp. 237-243
-
-
Bischoff, F.1
Nguyen, D.2
Burt, K.3
-
33
-
-
0027372861
-
Non-disjunction in human sperm: Results of fluorescence in situ hybridization studies using two and three probes
-
Williams B, Ballenger C, Malter H, et al.: Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Hum Mol Genet 1993;2:1929- 1936
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1929-1936
-
-
Williams, B.1
Ballenger, C.2
Malter, H.3
-
34
-
-
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 1995;42:89-93
-
(1995)
Mol Reprod Dev
, vol.42
, pp. 89-93
-
-
Martin, R.1
Rademaker, A.2
-
35
-
-
0029016039
-
Aneuploidy in human sperm: Results of two- And three-colour 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-colour fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X and Y. Cytogenet Cell Genet 1995;71:47-53
-
(1995)
Cytogenet Cell Genet
, vol.71
, pp. 47-53
-
-
Spriggs, E.1
Rademaker, A.2
Martin, R.3
-
36
-
-
0028818839
-
The relationship between paternal age, sex ratios and aneuploidy frequencies in human sperm as assessed by multicolour fluorescence in situ hybridization
-
Martin R, Spriggs E, Ko E, et al: The relationship between paternal age, sex ratios and aneuploidy frequencies in human sperm as assessed by multicolour fluorescence in situ hybridization. Am J Hum Genet 1995;57:1395-1399
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1395-1399
-
-
Martin, R.1
Spriggs, E.2
Ko, E.3
-
37
-
-
0030045646
-
Multicolour fluorescence in situ hybridization analysis of aneuploidy and diploidy frequencies in 225,846 sperm from ten normal men
-
Martin R, Spriggs E, Rademaker A: Multicolour fluorescence in situ hybridization analysis of aneuploidy and diploidy frequencies in 225,846 sperm from ten normal men. Biol Reprod 1996;54:394-398
-
(1996)
Biol Reprod
, vol.54
, pp. 394-398
-
-
Martin, R.1
Spriggs, E.2
Rademaker, A.3
-
38
-
-
0030052506
-
Aneuploidy in human sperm: The use of multicolour fluorescence in situ hybridization (FISH) to test various theories of nondisjunction
-
Spriggs E, Rademaker A, Martin R: Aneuploidy in human sperm: The use of multicolour fluorescence in situ hybridization (FISH) to test various theories of nondisjunction. Am J Hum Genet 1996;58:356-362
-
(1996)
Am J Hum Genet
, vol.58
, pp. 356-362
-
-
Spriggs, E.1
Rademaker, A.2
Martin, R.3
-
39
-
-
0029985631
-
Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in situ hybridization
-
Blanco J, Egozcue J, Vidal F: Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in situ hybridization. Hum Reprod 1996;11:722-726
-
(1996)
Hum Reprod
, vol.11
, pp. 722-726
-
-
Blanco, J.1
Egozcue, J.2
Vidal, F.3
-
40
-
-
0028030585
-
The origin of 47,XXY and 47,XXX aneuploidy heterogeneous mechanisms and role of aberrant recombination
-
MacDonald M, Hassold T, Harvey J, et al.: The origin of 47,XXY and 47,XXX aneuploidy heterogeneous mechanisms and role of aberrant recombination. Hum Mol Genet 1994;3: 1365-1371
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1365-1371
-
-
MacDonald, M.1
Hassold, T.2
Harvey, J.3
-
41
-
-
0030671186
-
Paternal age effect of YY aneuploidy in human sperm assessed by fluorescence in situ hybridization
-
Kinakin B, Rakemaker A, Martin RH: Paternal age effect of YY aneuploidy in human sperm assessed by fluorescence in situ hybridization. Cytogenet Cell Genet 1997;78(2):116-119
-
(1997)
Cytogenet Cell Genet
, vol.78
, Issue.2
, pp. 116-119
-
-
Kinakin, B.1
Rakemaker, A.2
Martin, R.H.3
-
42
-
-
0028792586
-
Non-disjunction in human sperm: Evidence for an effect of increasing age
-
Griffin D, Abruzzo M, Millie E, Sheean L, Feingold E, Sherman S, et al.: Non-disjunction in human sperm: Evidence for an effect of increasing age. Hum Mol Genet 1995;4:2227-2232
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2227-2232
-
-
Griffin, D.1
Abruzzo, M.2
Millie, E.3
Sheean, L.4
Feingold, E.5
Sherman, S.6
-
43
-
-
0029456938
-
Three probe FISH to assess chromosome X,Y, and 8 aneuploidy in sperm of 14 men from two healthy groups: Evidence for a paternal age effect on sperm aneuploidy
-
Robbins W, Baulch J, Moore D, Weier H, Blakey D, Wyrobek A: Three probe FISH to assess chromosome X,Y, and 8 aneuploidy in sperm of 14 men from two healthy groups: Evidence for a paternal age effect on sperm aneuploidy. Reprod Fertil Dev 1995; 7:799-809.
-
(1995)
Reprod Fertil Dev
, vol.7
, pp. 799-809
-
-
Robbins, W.1
Baulch, J.2
Moore, D.3
Weier, H.4
Blakey, D.5
Wyrobek, A.6
-
44
-
-
0028818839
-
The relationship between paternal age, sex ratios and aneuploidy frequencies in human sperm as assessed by multicolour fluorescence in situ hybridization
-
Martin R, Spriggs E, Ko E, Rademaker A: The relationship between paternal age, sex ratios and aneuploidy frequencies in human sperm as assessed by multicolour fluorescence in situ hybridization. Am J Hum Genet 1995;57:1395-1399
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1395-1399
-
-
Martin, R.1
Spriggs, E.2
Ko, E.3
Rademaker, A.4
-
45
-
-
0027474493
-
Potential genetic risks of using semen collected during chemotherapy
-
Meistrich M: Potential genetic risks of using semen collected during chemotherapy. Hum Reprod 1993;8:8-10
-
(1993)
Hum Reprod
, vol.8
, pp. 8-10
-
-
Meistrich, M.1
-
46
-
-
0023263285
-
Chromosome analysis of human sperm. I. First results with a modified method
-
Jenderny J, Rohrborn G: Chromosome analysis of human sperm. I. First results with a modified method. Hum Genet 1987;76:385-388
-
(1987)
Hum Genet
, vol.76
, pp. 385-388
-
-
Jenderny, J.1
Rohrborn, G.2
-
47
-
-
0025010591
-
Significance of structural chromosome aberrations in human sperm: Analysis of induced aberrations
-
Genesca A, Benet J, Caballin M, et al.: Significance of structural chromosome aberrations in human sperm: Analysis of induced aberrations. Hum Genet 1990;85:495-499
-
(1990)
Hum Genet
, vol.85
, pp. 495-499
-
-
Genesca, A.1
Benet, J.2
Caballin, M.3
-
48
-
-
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 B, Meistrich M, Gordon L, et al.: 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 1994;93:295-299
-
(1994)
Hum Genet
, vol.93
, pp. 295-299
-
-
Brandriff, B.1
Meistrich, M.2
Gordon, L.3
-
49
-
-
0026801137
-
Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patients
-
Jenderny J, Jacobi M, Ruger A, Rohrborn G: Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patients. Hum Genet 1992;90:151-154
-
(1992)
Hum Genet
, vol.90
, pp. 151-154
-
-
Jenderny, J.1
Jacobi, M.2
Ruger, A.3
Rohrborn, G.4
-
50
-
-
0030700504
-
Analysis of human sperm karyotypes in testicular cancer patients before and after chemotherapy
-
Martin RH, Ernst S, Rademaker A, Barclay L, Ko E, Summers N: Analysis of human sperm karyotypes in testicular cancer patients before and after chemotherapy. Cytogenet Cell Genet 1997;78:120-123
-
(1997)
Cytogenet Cell Genet
, vol.78
, pp. 120-123
-
-
Martin, R.H.1
Ernst, S.2
Rademaker, A.3
Barclay, L.4
Ko, E.5
Summers, N.6
-
51
-
-
0031028036
-
Chromosomal abnormalities in sperm from testicular cancer patients before and after chemotherapy
-
Martin R, Ernst S, Rademaker A, et al.: Chromosomal abnormalities in sperm from testicular cancer patients before and after chemotherapy. Hum Genet 1997;99:214-218
-
(1997)
Hum Genet
, vol.99
, pp. 214-218
-
-
Martin, R.1
Ernst, S.2
Rademaker, A.3
-
52
-
-
0028823335
-
Sex chromosome abnormalities after intracytoplasmic sperm injection
-
Liebaers I, Bonduelle M, van Assche E, et al.: Sex chromosome abnormalities after intracytoplasmic sperm injection. Lancet 1995;346:1095
-
(1995)
Lancet
, vol.346
, pp. 1095
-
-
Liebaers, I.1
Bonduelle, M.2
Van Assche, E.3
-
53
-
-
0029087947
-
Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping in situ hybridization
-
Moosani N, Pattinson H, Carter M, et al.: Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping in situ hybridization. Fertil Steril 1995;64:811-817
-
(1995)
Fertil Steril
, vol.64
, pp. 811-817
-
-
Moosani, N.1
Pattinson, H.2
Carter, M.3
-
54
-
-
0001149670
-
Detection by fluorescence in situ hybridisation of chromosome 7, 11, 12, 18, X and Y abnormalities in sperm from oligoasthenospermic patients of an in vitro fertilisation program
-
Pang M, Zackowski J, Hoegerman S, et al.: Detection by fluorescence in situ hybridisation of chromosome 7, 11, 12, 18, X and Y abnormalities in sperm from oligoasthenospermic patients of an in vitro fertilisation program. J Assist Reprod Genet 1995;12:53S
-
(1995)
J Assist Reprod Genet
, vol.12
-
-
Pang, M.1
Zackowski, J.2
Hoegerman, S.3
-
55
-
-
0028269490
-
Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization
-
Miharu N, Best R, Young S: Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization. Hum Genet 1994;93: 502-506
-
(1994)
Hum Genet
, vol.93
, pp. 502-506
-
-
Miharu, N.1
Best, R.2
Young, S.3
-
56
-
-
0021058956
-
Meiotic studies in a series of 1100 infertile and sterile males
-
Egozcue J, Templado C, Vidal F, et al.: Meiotic studies in a series of 1100 infertile and sterile males. Hum Genet 1983;65:185-188
-
(1983)
Hum Genet
, vol.65
, pp. 185-188
-
-
Egozcue, J.1
Templado, C.2
Vidal, F.3
-
57
-
-
0025220142
-
Prophase of meiosis in human spermatocytes analyzed by EM microspreading in infertile men and their controls and comparisons with human oocytes
-
Speed R. Chandley A: Prophase of meiosis in human spermatocytes analyzed by EM microspreading in infertile men and their controls and comparisons with human oocytes. Hum Genet 1990;84:547-554
-
(1990)
Hum Genet
, vol.84
, pp. 547-554
-
-
Speed, R.1
Chandley, A.2
-
58
-
-
0026334334
-
XY chromosome non- Disjunction in man is associated with diminished recombination in the pseudoautosomal region
-
Hassold T, Sherman S, Pettay D, et al.: XY chromosome non- disjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet 1991;49: 253-260
-
(1991)
Am J Hum Genet
, vol.49
, pp. 253-260
-
-
Hassold, T.1
Sherman, S.2
Pettay, D.3
|