Oculoauriculovertebral spectrum: Report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature

Clinical Dysmorphology

Volumn 18, Issue 2, 2009, Pages 67-77

  Vendramini Pittoli, Siulan ^a   Kokitsu Nakata, Nancy Mizue ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Autosomal dominant inheritance; First and second branchial arches; Goldenhar syndrome; Hemifacial microsomia; Oculoauriculovertebral dysplasia; Oculoauriculovertebral spectrum; Vendramini Pittoli and Kokitsu Nakata

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLINICAL FEATURE; CONSANGUINITY; CONTROLLED STUDY; FACE ASYMMETRY; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; GOLDENHAR SYNDROME; HUMAN; INFANT; MALE; PRIORITY JOURNAL; ADOLESCENT; CASE REPORT; DOMINANT GENE; FAMILY; GENETICS; MULTIPLE MALFORMATION SYNDROME; PRESCHOOL CHILD; REVIEW;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; FAMILY; FEMALE; GENES, DOMINANT; GOLDENHAR SYNDROME; HUMANS; INFANT; MALE;

EID: 66149108858     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e328323a7dd     Document Type: Article

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