Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome
- 1 May 1996
- journal article
- Published by Elsevier in The Lancet
- Vol. 347 (9011) , 1290-1293
- https://doi.org/10.1016/s0140-6736(96)90938-1
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Viable Embryos from Injection of Round Spermatids into OocytesNew England Journal of Medicine, 1995
- Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein geneNature Genetics, 1995
- PCR analysis of the Y chromosome long arm in azoospermic patients: evidence for a second locus required for spermatogenesisHuman Molecular Genetics, 1994
- A locus of the candidate gene family for azoospermia factor (YRRM2) is polymorphic with a null allele in Japanese malesHuman Molecular Genetics, 1994
- The Human Y Chromosome: A 43-Interval Map Based on Naturally Occurring DeletionsScience, 1992
- The Human Y Chromosome: Overlapping DNA Clones Spanning the Euchromatic RegionScience, 1992
- The sex-determining region of the human Y chromosome encodes a finger proteinCell, 1987
- Population study of causes, treatment, and outcome of infertility.BMJ, 1985
- Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long armHuman Genetics, 1976
- Quinacrine Fluorescence of the Human Y ChromosomeNature, 1971