Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference18 articles.
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2. Oligozoospermia: a seven-year survey of the incidence, chromosomal aberrations, treatment and pregnancy rate;van Zyl;Int J Fertil,1975
3. Localization of factors controlling spermatogenesis in the non-fluorescent portion of the human Y chromosome long arm;Tiepolo;Hum Genet,1976
4. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene;Reijo;Nature Genet,1995
5. A locus of the candidate gene family for azoospermia factor (YRRM2) is polymorphic with a null allele in Japanese males;Nakahori;Hum Molec Genet,1994
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