Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian population

Osteoarthritis and Cartilage

Volumn 17, Issue 8, 2009, Pages 1099-1105

  Rouault, K ^a,b,c,d   Scotet, V ^a,b,c   Autret, S ^a,b,c   Gaucher, F ^e   Dubrana, F ^f   Tanguy, D ^g   Yaacoub El Rassi, C ^h   Fenoll, B ^d   Ferec C ^a,b,c,d  

^a INSERM   (France)

^b FACULTÉ DE MÉDECINE ET DES SCIENCES DE LA SANTÉ   (France)

^c ETABLISSEMENT FRANÇAIS DU SANG   (France)

^d CHU MORVAN   (France)

^e Service de chirurgie orthopédique   (France)

^f BREST UNIVERSITY HOSPITAL   (France)

^g Centre de Perharidy   (France)

^h CH Quimper   (France)

Author keywords

Association study; Candidate genes; Case control study; COL1A1; Congenital dislocation of the hip; HOXB9; Transmission disequilibrium test

Indexed keywords

COLLAGEN; COLLAGEN TYPE 1A1; HOXB9 PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; CAUCASIAN; CHROMOSOME 17; CONGENITAL HIP DISLOCATION; CONTROLLED STUDY; FEMALE; FRANCE; GENE FUNCTION; GENE LOCUS; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; POPULATION BASED CASE CONTROL STUDY; POPULATION GENETICS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; COLLAGEN TYPE I; FEMALE; FRANCE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOTYPE; HAPLOTYPES; HIP DISLOCATION, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; MALE; POLYMORPHISM, GENETIC; RISK FACTORS;

EID: 67650409976     PISSN: 10634584     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.joca.2008.12.012     Document Type: Article

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