Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia
- 1 April 1999
- journal article
- Published by Elsevier in Fertility and Sterility
- Vol. 71 (4) , 697-700
- https://doi.org/10.1016/s0015-0282(98)00535-4
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- ANDROGEN RECEPTOR GENE ALTERATIONS ARE NOT ASSOCIATED WITH ISOLATED CRYPTORCHIDISMJournal of Urology, 1998
- Paternity After Bilateral CryptorchidismArchives of Pediatrics & Adolescent Medicine, 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
- Sexually dimorphic sterility phenotypes in HoxalO-deficient miceNature, 1995
- The Human Y Chromosome: A 43-Interval Map Based on Naturally Occurring DeletionsScience, 1992
- A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesisGenomics, 1991
- Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11Human Genetics, 1988
- Testicular Function after Orchiopexy for Unilaterally Undescended TestisNew England Journal of Medicine, 1976
- Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long armHuman Genetics, 1976