Understanding the Y chromosome.
- 1 November 1999
- journal article
- editorial
- Published by Elsevier in The Lancet
- Vol. 354 (9192) , 1746-1747
- https://doi.org/10.1016/s0140-6736(99)00311-6
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extractionHuman Reproduction, 1998
- Understanding the Genes Involved in Spermatogenesis: A Progress ReportFertility and Sterility, 1998
- Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry geneHuman Molecular Genetics, 1998
- The testis: the witness of the mating system, the site of mutation and the engine of desireActa Paediatrica, 1997
- Microdeletions in the Y Chromosome of Infertile MenNew England Journal of Medicine, 1997
- 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 Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesisCell, 1993
- Towards the molecular localisation of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosomeHuman Molecular Genetics, 1992
- Genetic evidence equating SRY and the testis-determining factorNature, 1990