Positive association of the FTSJ1 gene polymorphisms with nonsyndromic X-linked mental retardation in young Chinese male subjects

Journal of Human Genetics

Volumn 53, Issue 7, 2008, Pages 592-597

  Dai, Ling ^a   Xing, Lianxi ^a   Gong, Pingyuan ^a   Zhang, Kejin ^a   Gao, Xiaocai ^a   Zheng, Zijian ^a   Zhou, Jianping ^b   Guo, Yale ^b   Guo, Shaoping ^b   Zhang, Fuchang ^a  

^a NORTHWEST UNIVERSITY   (China)

^b XI'AN JIAOTONG UNIVERSITY   (China)

Author keywords

Association study; FTSJ1; Haplotype analysis; Non syndromic X linked mental retardation (NS XLMR); Single nucleotide polymorphism (SNP)

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HIGH RISK POPULATION; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; SINGLE STRAND CONFORMATION POLYMORPHISM; STATISTICAL SIGNIFICANCE; X LINKED MENTAL RETARDATION;

ADOLESCENT; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CHINA; FEMALE; HAPLOTYPES; HUMANS; INFANT; INFANT, NEWBORN; MALE; MENTAL RETARDATION, X-LINKED; METHYLTRANSFERASES; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SYNDROME;

EID: 46149118194     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-008-0287-x     Document Type: Article

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