Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle

Clinical Genetics

Volumn 82, Issue 5, 2012, Pages 466-471

  Tan, Z P ^a,b   Huang, C ^b   Xu, Z B ^b   Yang, J F ^a,b   Yang, Y F ^a,b  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Congenital heart defect; Double outlet right ventricle; FOG2; Mutation; ZFPM2

Indexed keywords

ARTICLE; CHILD; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CONTROLLED STUDY; GENE; GENE LOCUS; GENE SEQUENCE; GENETIC VARIABILITY; HEART RIGHT VENTRICLE DOUBLE OUTLET; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; ZFPM 2 GENE;

ADOLESCENT; AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN; COHORT STUDIES; DNA-BINDING PROTEINS; DOUBLE OUTLET RIGHT VENTRICLE; EXONS; FEMALE; GENE DELETION; GENE FREQUENCY; GENETIC LOCI; GENETIC VARIATION; HERNIA, DIAPHRAGMATIC; HUMANS; KARYOTYPING; MALE; MOLECULAR SEQUENCE DATA; MUTATION; SEQUENCE ANALYSIS, DNA; TETRALOGY OF FALLOT; TRANSCRIPTION FACTORS;

EID: 84867652053     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2011.01787.x     Document Type: Article

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