Meiotic segregation in spermatozoa of a 46,X,t(Y;10)(q11.2;p15.2) fertile translocation carrier

Author:

Vialard F,Molina-Gomes D,Roume J,Podbiol A,Hirel C,Bailly M,Hammoud I,Dupont JM,de Mazancourt P,Selva J

Publisher

Elsevier BV

Subject

Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology

Reference25 articles.

1. An excess of chromosome 1 breakpoints in male infertility;Bache;European Journal of Human Genetics,2004

2. Segregation of chromosomes in sperm of reciprocal translocation carriers: a review;Benet;Cytogenetics and Genome Research,2005

3. [Chromosome anomalies and male infertility. A study of 1,444 subjects];Bourrouillou;Bulletin Association Anatomie (Nancy),1987

4. Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report;Brisset;Human Reproduction,2005

5. A simplified method for the detection of Y chromosome microdeletions in infertile men using a multiplex sequence-tagged site-based amplification;Charpenel;Genetic Testing,2002

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