A Deficiency in the Region Homologous to Human 17q21.33–q23.2 Causes Heart Defects in Mice

Several constitutional chromosomal rearrangements occur on human chromosome 17. Patients who carry constitutional deletions of 17q21.3–q24 exhibit distinct phenotypic features. Within the deletion interval, there is a genomic segment that is bounded by the myeloperoxidase and homeobox B1 genes. This...

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Bibliographic Details
Main Authors: Yu, Y. Eugene, Morishima, Masae, Pao, Annie, Wang, Ding-Yan, Wen, Xiao-Yan, Baldini, Antonio, Bradley, Allan
Format: Artigo
Language:Inglês
Published: Copyright © 2006 by the Genetics Society of America 2006
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Investigations
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1461454/
https://ncbi.nlm.nih.gov/pubmed/16489219
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.105.054833
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