Dominant inheritance of cleft palate, microstomia and micrognathia - Possible linkage to the fragile site at 16q22 (FRA16B)

Clinical Dysmorphology

Volumn 11, Issue 4, 2002, Pages 237-241

  McKenzie, F ^a   Turner, A ^a   Withers, S ^a   Dalzell, P ^a   McGlynn, M ^a   Kirk, Edwin P E ^a  

^a SYDNEY CHILDREN'S HOSPITAL   (Australia)

Author keywords

Chromosome 16q22 fragile site; Cleft palate; Micrognathia; Microstomia

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 16Q; CHROMOSOME FRAGILE SITE; CLEFT PALATE; CLINICAL FEATURE; CYTOGENETICS; DOMINANT INHERITANCE; FEMALE; GENETIC LINKAGE; HUMAN; KARYOTYPE; MALE; MICROGNATHIA; MICROSTOMIA; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0036791241     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200210000-00002     Document Type: Article

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