Transmissible microdeletion of the Y-chromosome encompassing two DAZ copies, four RBMY1 copies, and both PRY copies
- 31 December 2010
- journal article
- case report
- Published by Elsevier BV in Fertility and Sterility
- Vol. 94 (7), 2770.e11-2770.e16
- https://doi.org/10.1016/j.fertnstert.2010.04.038
Abstract
No abstract availableKeywords
Funding Information
- Hospices Civils de Lyon
This publication has 27 references indexed in Scilit:
- The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile menNature Genetics, 2001
- Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY) assessed by fluorescence in-situ hybridization*Human Reproduction, 2001
- Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events.Human Molecular Genetics, 2000
- Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11Human Molecular Genetics, 1996
- Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein geneNature Genetics, 1995
- A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesisCell, 1993
- 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
- Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis geneHuman Genetics, 1992
- Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long armHuman Genetics, 1976