Are Sequence Family Variants Useful for Identifying Deletions in the Human Y Chromosome?
- 1 September 2004
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 75 (3), 514-517
- https://doi.org/10.1086/423394
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c regionGenomics, 2004
- A Large AZFc Deletion Removes DAZ3/DAZ4 and Nearby Genes from Men in Y Haplogroup NAmerican Journal of Human Genetics, 2004
- Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selectionNature Genetics, 2003
- Abundant gene conversion between arms of palindromes in human and ape Y chromosomesNature, 2003
- The male-specific region of the human Y chromosome is a mosaic of discrete sequence classesNature, 2003
- High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermiaMolecular Human Reproduction, 2002
- A Nomenclature System for the Tree of Human Y-Chromosomal Binary HaplogroupsGenome Research, 2002
- The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile menNature Genetics, 2001
- Y chromosome sequence variation and the history of human populationsNature Genetics, 2000
- Four DAZ Genes in Two Clusters Found in the AZFc Region of the Human Y ChromosomeGenomics, 2000