Adams-Oliver syndrome: Clinical description of a four-generation family and exclusion of five candidate genes

Clinical Genetics

Volumn 69, Issue 1, 2006, Pages 86-92

  Verdyck, P ^a   Blaumeiser, B ^a   Holder Espinasse, M ^b   Van Hul, W ^a   Wuyts, Wim ^a  

^a ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Adams; Aplasia cutis; CART1; HOXD13; MSX1; Oliver syndrome; P63; RUNX2

Indexed keywords

HOX PROTEIN; HOXD13 PROTEIN; ISOPROTEIN; PROTEIN P63; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR RUNX2; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED FACTOR 4; UNCLASSIFIED DRUG;

ADAMS OLIVER SYNDROME; ALOPECIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BELGIUM; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; EXON; FAMILIAL DISEASE; FEMALE; GENE AMPLIFICATION; GENETIC PREDISPOSITION; HUMAN; LIMB REDUCTION DEFECT; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SYMPTOMATOLOGY; TOE MALFORMATION;

DNA MUTATIONAL ANALYSIS; ECTODERMAL DYSPLASIA; FAMILY HEALTH; FEMALE; GENES, DOMINANT; HUMANS; LIMB DEFORMITIES, CONGENITAL; MALE; PEDIGREE; PHENOTYPE; SYNDROME;

EID: 33644861426     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2006.00552.x     Document Type: Article

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