De novo chromosomal translocation t(3;5)(q13;q35) in an infertile man

Author:

Venkateshwari A.,Srilekha A.,Begum A.,Sujatha M.,Sunitha T.,Nallari P.,Jyothy A.

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Reference10 articles.

1. A human 9;20 translocation associated with male infertility analysed at prophase and metaphase I of meiosis;Chandley;Cytogenet Cell Genet,1986

2. Cytogenetic studies in male infertility a review;De Brakeleer;Hum Reprod,1991

3. Two familial 9;17 translocations with variable effect on male carriers fertility;Debiec-Rychter;Fertil Steril,1992

4. Increased incidence of meiotic anomalies in oligoasthenozoospermic males preselected for intracytoplasmic sperm injection;Egozcue;J Asst Reprod Genet,2000

5. The meiotic pairing behaviour in human spermatocytes carrier of chromosome anomalies and their repercussions on reproductive fitness. II. Robertsonian and reciprocal translocations. A European collaborative study;Gabriel-Robez;Ann Genet,1996

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