Screening NKX2.5 mutation in a sample of 230 Han Chinese children with congenital heart diseases.

Genetic testing and molecular biomarkers

Volumn 13, Issue 2, 2009, Pages 159-162

  Zhang, Weimin ^a   Li, Xiaofeng ^a   Shen, Adong ^a   Jiao, Weiwei ^a   Guan, Xiaolei ^a   Li, Zhongzhi ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; NKX2 5 PROTEIN, HUMAN; NKX2-5 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ALLELE; ARTICLE; ASIAN; CHINA; COHORT ANALYSIS; CONGENITAL HEART MALFORMATION; DNA SEQUENCE; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENETICS; HEART SEPTUM DEFECT; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD, PRESCHOOL; CHINA; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC SCREENING; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, VENTRICULAR; HOMEODOMAIN PROTEINS; HUMANS; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; TRANSCRIPTION FACTORS;

EID: 67650033423     PISSN: None     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2008.0044     Document Type: Article

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