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Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

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Year: 2002
Type: article
Source: Human Molecular Genetics
DOI: 10.1093/hmg/11.8.915
Author: F. Vitelli
Institution: Baylor College of Medicine
Language: English

Topic: Congenital heart defects research
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: American Heart Association, National Heart, Lung, and Blood Institute
Awards: G1507758581, G2310128481, G3251825224, Molecular Cytogenetics of Congenital Heart Malformation, Identification and Characterization of Genes from del22q, Development/Genetic Aspects of Congenital Heart Disease
OpenAlex ID: W2011884985
FWCI: 8.46
Cites: 26
Cited by: 330
Related to: 10
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