Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

Human Molecular Genetics

Volumn 10, Issue 2, 2001, Pages 163-169

  Eldadah, Zayd A ^a   Hamosh, Ada ^a   Biery, Nancy J ^a   Montgomery, Robert A ^a   Duke, Melinda ^b   Elkins, Ronald ^c   Dietz, Harry C ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MARYLAND MEDICAL CENTER   (United States)

^c UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EPIDERMAL GROWTH FACTOR; GLYCINE; LIGAND; NOTCH RECEPTOR;

ADULT; ALAGILLE SYNDROME; AMINO ACID SUBSTITUTION; AORTA ANOMALY; ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FALLOT TETRALOGY; FAMILIAL DISEASE; FAMILY; FEMALE; GENE MUTATION; GENETIC CONSERVATION; HEART DISEASE; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOTE; HUMAN; JAW MALFORMATION; MALE; NOSE MALFORMATION; PALPEBRAL FISSURE ANOMALY; PATHOGENESIS; PRIORITY JOURNAL; PULMONARY ARTERY ATRESIA; PULMONARY VALVE; PULMONARY VALVE STENOSIS; TOOTH ARCH;

EID: 0035862854     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.2.163     Document Type: Article

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