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Volumn 98, Issue 3, 2001, Pages 224-229

Haplotype analysis at the FRAXA locus in Thai subjects

(7) Limprasert, Pornprot a Saechan, Vannarat b Ruangdaraganon, Nichara c Sura, Thanyachai d Vasiknanote, Punnee d Jaruratanasirikul, Somchit d Ted Brown, W d

a PRINCE OF SONGKLA UNIVERSITY (Thailand)

b MAHIDOL UNIVERSITY (Thailand)

c NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES (United States)

d UNIVERSITY OF WASHINGTON (United States)

Author keywords

FMR1; Founder effects; Haplotype; Microsatellite; SNPs

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; GENE PRODUCT; MICROSATELLITE DNA; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ETHNIC DIFFERENCE; FOUNDER EFFECT; FRAGILE X SYNDROME; GENE LOCATION; GENE LOCUS; GENE MUTATION; HAPLOTYPE; HUMAN; MALE; MARKER GENE; MICROSATELLITE INSTABILITY; PREVALENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; THAILAND;

ALLELES; BLOTTING, SOUTHERN; DNA; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; GENE FREQUENCY; HAPLOTYPES; HUMANS; MICROSATELLITE REPEATS; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; RNA-BINDING PROTEINS; THAILAND; TRINUCLEOTIDE REPEATS;

EID: 0035931390 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(20010122)98:3<224::AID-AJMG1096>3.0.CO;2-R Document Type: Article

Times cited : (11)

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