Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot

American Journal of Medical Genetics, Part A

Volumn 149, Issue 12, 2009, Pages 2745-2752

  Ester, Audrey R ^a   Weymouth, Katelyn S ^a   Burt, Amber ^b   Wise, Carol A ^c   Scott, Allison ^d   Gurnett, Christina A ^e   Dobbs, Matthew B ^e   Blanton, Susan H ^b   Hecht, Jacqueline T ^a,d  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^c TEXAS SCOTTISH RITE HOSPITAL FOR CHILDREN   (United States)

^d Shriners Hospital for Children   (United States)

^e WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Association study; Clubfoot; Complex disease; Genotyping; HOXA; IGFBP3

Indexed keywords

SOMATOMEDIN BINDING PROTEIN 3;

ADOLESCENT; ADULT; APOPTOSIS; ARTICLE; CHILD; CLUBFOOT; CONTROLLED STUDY; FEMALE; GENE CLUSTER; GENE EXPRESSION; GENE FREQUENCY; GENE FUNCTION; GENE INTERACTION; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HOX GENE; HOXA GENE; HOXD GENE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MORPHOGENESIS; MUSCLE DEVELOPMENT; PRESCHOOL CHILD; PRIORITY JOURNAL; PROMOTER REGION; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

APOPTOSIS; BINDING SITES; CLUBFOOT; GENE FREQUENCY; HAPLOTYPES; HISPANIC AMERICANS; HOMEODOMAIN PROTEINS; HUMANS; INHERITANCE PATTERNS; INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN 3; LINKAGE (GENETICS); MITOCHONDRIA; MODELS, GENETIC; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; SIGNAL TRANSDUCTION; TRANSCRIPTION FACTORS;

EID: 71949129199     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33130     Document Type: Article

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