Growth hormone deficiency in patients with a 22q11.2 deletion: Expanding the phenotype

Pediatrics

Volumn 101, Issue 5, 1998, Pages 929-932

  Weinzimer, Stuart A ^a   McDonald McGinn, Donna M ^a   Driscoll, Deborah A ^a,b   Emanuel, Beverly S ^a   Zackai, Elaine H ^a   Moshang Jr , Thomas ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

22q11.2 deletion; Deficiency; DiGeorge sequence; Growth hormone; Short stature; Velocardiofacial syndrome

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CHILD GROWTH; CHROMOSOME 22Q; DIGEORGE SYNDROME; FEMALE; GENE DELETION; GROWTH HORMONE DEFICIENCY; HUMAN; MALE; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE; VELOCARDIOFACIAL SYNDROME;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENE DELETION; GROWTH DISORDERS; HUMAN GROWTH HORMONE; HUMANS; MALE; PHENOTYPE;

EID: 0031924716     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.101.5.929     Document Type: Article

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