Syndromic foramina parietalia permagna

American Journal of Medical Genetics

Volumn 78, Issue 5, 1998, Pages 401-405

  Chrzanowska, Krystyna ^a   Kozlowski, Kazimierz ^a,b   Kowalska, Aleksandra ^b  

^a CHILDREN'S MEMORIAL HEALTH INSTITUTE   (Poland)

^b CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

Branchial syndrome; Face abnormalities; Foramina parietalia permagna

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRANCHIOOTORENAL SYNDROME; CASE REPORT; CHILD; FACE MALFORMATION; FISTULA; HUMAN; MALE; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; SKELETON MALFORMATION;

ABNORMALITIES, MULTIPLE; EAR; FACE; GENITALIA, MALE; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; MOUTH ABNORMALITIES; PARIETAL BONE; PHENOTYPE; SCOLIOSIS; SYNDROME; TOES;

EID: 0031826934     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980806)78:5<401::AID-AJMG1>3.0.CO;2-O     Document Type: Article

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