Identification of association of common AGGF1 variants with susceptibility for klippel-trenaunay syndrome using the structure association program

Annals of Human Genetics

Volumn 72, Issue 5, 2008, Pages 636-643

  Hu, Y ^a   Li, L ^a   Seidelmann, S B ^a   Timur, A A ^a   Shen, P H ^b   Driscoll, D J ^c   Wang, Qing Kenneth ^a,d,e  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM   (United States)

^c MAYO CLINIC   (United States)

^d HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^e LERNER RESEARCH INSTITUTE   (United States)

Author keywords

AGGF1 (VG5Q); Ancestry informative markers (AIMs); Case control association study; Klippel Trenaunay Syndrome (KTS); Linkage disequilibrium (LD) block; Single nucleotide polymorphism (SNP); Structured association

Indexed keywords

ANGIOGENIC FACTOR; ANGIOGENIC FACTOR WITH G PATCH AND FHA DOMAIN 1;

ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CAUCASIAN; COMPUTER PROGRAM; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE MAP; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIVARIATE ANALYSIS; NUCLEOTIDE SEQUENCE; PLESIOMORPHY; POPULATION STRUCTURE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE;

ANGIOGENIC PROTEINS; CASE-CONTROL STUDIES; DATABASES, GENETIC; EXONS; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INTRONS; KLIPPEL-TRENAUNAY-WEBER SYNDROME; MALE; MODELS, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; SOFTWARE; VARIATION (GENETICS);

EID: 49449083991     PISSN: 00034800     EISSN: 14691809     Source Type: Journal    
DOI: 10.1111/j.1469-1809.2008.00458.x     Document Type: Article

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