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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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Puech, Anne, Saint-Jore, Bruno, Merscher, Sandra, Russell, Robert G., Cherif, Dorra, Sirotkin, Howard, Xu, Hui, Factor, Stephen, Kucherlapati, Raju, Skoultchi, Arthur I.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 2000
Assuntos:	Biological Sciences
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC27709/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10963672/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.97.18.10090
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