Association of the GLI gene with ventricular septal defect after the susceptibility gene being narrowed to 3.56 cM in 12q13

Chinese Medical Journal

Volumn 119, Issue 4, 2006, Pages 267-274

  Qiu, Guang Rong ^a   Gong, Li Guo ^a   He, Guang ^a   Xu, Xiao Yan ^a   Xin, Na ^a   Sun, Gui Feng ^a   Yuan, Yi Hua ^a   Sun, Kai Lai ^a  

^a CHINA MEDICAL UNIVERSITY   (China)

Author keywords

Association study; GLI gene; Haplotype analysis; Transmission disequilibrium test; Ventricular septal defect

Indexed keywords

GENOMIC DNA; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GLI; UNCLASSIFIED DRUG; GLI PROTEIN, HUMAN; MICROSATELLITE DNA;

ARTICLE; CHILD; CHROMOSOME 12Q; CHROMOSOME MAP; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE ASSIGNMENT; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HUMAN CELL; LEUKOCYTE; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE MARKER; NUCLEAR FAMILY; PATHOGENESIS; SINGLE NUCLEOTIDE POLYMORPHISM; CHROMOSOME 12; GENETIC PREDISPOSITION; GENETICS; HEART SEPTUM DEFECT; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MICROSATELLITE REPEATS; TRANSCRIPTION FACTORS;

EID: 33645283126     PISSN: 03666999     EISSN: None     Source Type: Journal    
DOI: 10.1097/00029330-200602020-00001     Document Type: Article

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