Genomic disorders on chromosome 22
Abstract
Purpose of review Chromosome 22, the first human chromosome to be completely sequenced, is prone to genomic alterations. Copy-number variants (CNVs) are common because of an enrichment of low-copy repeat sequences that precipitate a high frequency of nonallelic homologous misalignments and unequal recombination during meiosis. Among these is one of the most common multiple anomaly syndromes in humans and the most common microdeletion syndrome,...
Paper Details
Title
Genomic disorders on chromosome 22
Published Date
Dec 1, 2012
Volume
24
Issue
6
Pages
665 - 671
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