Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/ DiGeorge syndrome region

Hemizygous interstitial deletions in human chromosome 22q11 are associated with velocardiofacial syndrome and DiGeorge syndrome and lead to multiple congenital abnormalities, including cardiovascular defects. The gene(s) responsible for these disorders is thought to reside in a 1.5-Mb region of 22q1...

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Detaylı Bibliyografya
Asıl Yazarlar: Puech, Anne, Saint-Jore, Bruno, Merscher, Sandra, Russell, Robert G., Cherif, Dorra, Sirotkin, Howard, Xu, Hui, Factor, Stephen, Kucherlapati, Raju, Skoultchi, Arthur I.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The National Academy of Sciences 2000
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC27709/
https://ncbi.nlm.nih.gov/pubmed/10963672
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