Structural variation of the human genome: mechanisms, assays, and role in male infertility
Author:
Publisher
Informa UK Limited
Subject
Urology,Reproductive Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/19396368.2010.527427
Reference116 articles.
1. Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11
2. A human Y-chromosomal DNA sequence expressed in testicular tissue
3. Dynamic nature of the proximalAZFcregion of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis
4. The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats
5. LINE-1 Retrotransposition Activity in Human Genomes
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