Sperm segregation analysis of a complex chromosome rearrangement, 2;22;11, by whole chromosome painting.

作者: P. Cifuentes , J. Navarro , L. Míguez , J. Egozcue , J. Benet

DOI: 10.1159/000015101

关键词:

摘要: Abstract. Using the human sperm–hamster oocyte fusion technique and whole chromosome painting, we studied sperm segregation in a male heterozygous for complex rear

参考文章(28)
M. A. Hulten, A. S. H. Goldman, J. Burn, R. H. Martin, J. E. Emslie, R. Johannisson, E. V. Davison, C. P. Gould, Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13). Journal of Medical Genetics. ,vol. 29, pp. 460- 464 ,(1992)
Stylianos E Antonarakis, Michael B Petersen, Melvin G McInnis, Patricia A Adelsberger, Albert A Schinzel, F Binkert, Constantine Pangalos, O Raoul, Susan A Slaugenhaupt, Mohamed Hafez, Maimon M Cohen, Diane Roulson, Stuart Schwartz, Margareta Mikkelsen, Lisbeth Tranebjaerg, Frank Greenberg, David I Hoar, Noreen L Rudd, Andrew C Warren, Caterina Metaxotou, Christos Bartsocas, Aravinda Chakravarti, The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms. American Journal of Human Genetics. ,vol. 50, pp. 544- 550 ,(1992)
J Navarro, J Egozcue, M R Martorell, J Benet, C Templado, Segregation analysis in a man heterozygous for a pericentric inversion of chromosome 7 (p13; q36) by sperm chromosome studies American Journal of Human Genetics. ,vol. 53, pp. 214- 219 ,(1993)
C. Templado, J. Navarro, R. Requena, J. Benet, F. Ballesta, J. Egozcue, Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36) Human Genetics. ,vol. 84, pp. 159- 162 ,(1990) , 10.1007/BF00208932
T. Ohta, T. Tohma, H. Soejima, Y. Fukushima, T. Nagai, K. Yoshiura, Y. Jinno, N. Niikawa, The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting. Human Genetics. ,vol. 92, pp. 1- 5 ,(1993) , 10.1007/BF00216136
R. D. Smart, A. E. Retief, Joan Overhauser, Confirmation of a balanced chromosomal translocation using molecular techniques. Prenatal Diagnosis. ,vol. 9, pp. 505- 513 ,(1989) , 10.1002/PD.1970090708
M. Fraccaro, J. Lindsten, C. E. Ford, L. Iselius, A. Antonelli, P. Aula, A. Aurias, A. D. Bain, M. Bartsch-Sandhoff, F. Bernardi, E. Boyd, L. F. Buchanan, A. H. Cameron, A. de la Chapelle, G. Ciuffa, C. Cuoco, B. Dutrillaux, G. Dutton, M. A. Ferguson-Smith, D. Francesconi, J. P. M. Geraedts, G. Gimelli, J. Gueguen, E. Gärsner, A. Hagemeijer, F. J. Hansen, P. E. Hollings, T. W. J. Hustinx, A. Kaakinen, J. J. P. van de Kamp, H. von Koskull, J. Lejeune, R. H. Lindenbaum, H. H. McCreanor, M. Mikkelsen, F. Mitelman, B. Nicoletti, J. Nilsby, B. Nilsson, B. Noel, E. Padovani, F. Pasquali, J. de Pater, C. Pedersen, F. Petersen, E. B. Robson, J. Rotman, M. Ryynänen, E. Sachs, J. Salat, R. H. Smythe, I. Stabell, I. Šubrt, P. Vampirelli, G. Wessner, L. Zergollern, O. Zuffardi, The 11q;22q translocation: A European collaborative analysis of 43 cases Human Genetics. ,vol. 56, pp. 21- 51 ,(1980) , 10.1007/BF00281567
Ren�eH. Martin, JudyE. Chernos, R.Brian Lowry, H.Anthony Pattinson, Leona Barclay, Evelyn Ko, Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1 Human Genetics. ,vol. 93, pp. 135- 138 ,(1994) , 10.1007/BF00210597
D. A. LAURIE, M. A. HULTÉN, Further studies on bivalent chiasma frequency in human males with normal karyotypes Annals of Human Genetics. ,vol. 49, pp. 189- 201 ,(1985) , 10.1111/J.1469-1809.1985.TB01693.X