A new syndrome: Heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs

Genetics in Medicine

Volumn 1, Issue 3, 1999, Pages 104-108

  Huang, Taosheng ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HIRSCHSPRUNG DISEASE; HUMAN; INFANT; KARYOTYPING; LARYNX; MALE; NUCLEAR FAMILY; POLYDACTYLY; PRESCHOOL CHILD; SYNDROME;

CHILD, PRESCHOOL; CYTOGENETIC ANALYSIS; FEMALE; HEART DEFECTS, CONGENITAL; HIRSCHSPRUNG DISEASE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; LARYNX; MALE; NUCLEAR FAMILY; POLYDACTYLY; SYNDROME;

EID: 0033086332     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/00125817-199903000-00008     Document Type: Article

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