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Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a JAG1 Mutation and/or Alagille Syndrome

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Year: 2002
Type: article
Study design: Observational Study
Source: Circulation
DOI: 10.1161/01.cir.0000037221.45902.69
Authors: Doff B. McElhinney, Ian D. Krantz, Lynn Bason, David A. Piccoli, Karan M. Emerick, Nancy B. Spinner, Elizabeth Goldmuntz
Institutions: Lurie Children's Hospital, Children's Hospital of Philadelphia, University of Pennsylvania
Language: English

Topic: Pediatric Hepatobiliary Diseases and Treatments
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: MOLECULAR ANALYSIS IN ALAGILLE SYNDROME, Molecular Analysis of Alagille Syndrome, GENETIC BASIS OF CONOTRUNCAL MALFORMATIONS
OpenAlex ID: W2116087542
FWCI: 10.66
Cites: 14
Cited by: 321
Related to: 10
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