Pulmonary agenesis: Expansion of the VCFS phenotype

American Journal of Medical Genetics

Volumn 113, Issue 1, 2002, Pages 89-92

  Conway, Karen ^a   Gibson, Ronald ^b   Perkins, Jonathan ^b   Cunningham, Michael L ^b  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

Carotid arteries; DiGeorge syndrome; Pulmonary agenesis; VCFS; Velocardiofacial syndrome

Indexed keywords

AORTA ARCH; ARTICLE; CASE REPORT; CELL MIGRATION; CHROMOSOME 22Q; CHROMOSOME DELETION; CLEFT PALATE; CLINICAL FEATURE; DIAGNOSTIC IMAGING; DIGEORGE SYNDROME; EMBRYO DEVELOPMENT; FACE MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; IMAGE ANALYSIS; LUNG AGENESIS; LUNG DEVELOPMENT; NEURAL CREST CELL; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM; THORAX RADIOGRAPHY; VELOCARDIOFACIAL SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; LUNG; PHENOTYPE; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0037110985     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10673     Document Type: Article

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