PubMed

Haplotype analysis at the FRAXA locus in Thai subjects.

Limprasert P, Saechan V, Ruangdaraganon N, Sura T, Vasiknanote P, Jaruratanasirikul S, Brown WT.

Am J Med Genet. 2001 Jan 22;98(3):224-9.PMID: 11169559 [PubMed - indexed for MEDLINE]Related articles

Validity of analysis of FMRP expression in blood smears as a screening test for Fragile X Syndrome in the Indian population.

Ravindran MS, Patel ZM, Adhia RA, D'souza AK, Babu S.

J Clin Lab Anal. 2005;19(3):120-3.PMID: 15900569 [PubMed - indexed for MEDLINE]Related articles

Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?

Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S.

Psychiatr Genet. 2001 Dec;11(4):201-5.PMID: 11807410 [PubMed - indexed for MEDLINE]Related articles

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.

Tzeng CC, Tsai LP, Hwu WL, Lin SJ, Chao MC, Jong YJ, Chu SY, Chao WC, Lu CL.

Am J Med Genet A. 2005 Feb 15;133A(1):37-43.PMID: 15637705 [PubMed - indexed for MEDLINE]Related articles

A step-wise diagnosis of fragile X syndrome in Taiwan.

Huang YT, Chiang SC, Tzeng CC, Liu CH, Chien YH, Hwu WL.

Acta Paediatr Taiwan. 2004 Mar-Apr;45(2):69-72.PMID: 15335113 [PubMed - indexed for MEDLINE]Related articles

[Polymorphism of trinucleotide repeats at loci FRAXA and FRAXE in the population of Tomsk]

Tolmacheva EN, Nazarenko SA.

Genetika. 2002 Feb;38(2):268-73. Russian. PMID: 11898618 [PubMed - indexed for MEDLINE]Related articles

Fragile X syndrome: a clinico-genetic study of mentally retarded patients in Kuwait.

Bastaki LA, Hegazy F, Al-Heneidi MM, Turki N, Azab AS, Naguib KK.

East Mediterr Health J. 2004 Jan-Mar;10(1-2):116-24.PMID: 16201716 [PubMed - indexed for MEDLINE]Related articles

Fragile X syndrome carrier screening in the prenatal genetic counseling setting.

Cronister A, DiMaio M, Mahoney MJ, Donnenfeld AE, Hallam S.

Genet Med. 2005 Apr;7(4):246-50.PMID: 15834242 [PubMed - indexed for MEDLINE]Related articles

Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.

Major T, Culjkovic B, Stojkovic O, Gucscekic M, Lakic A, Romac S.

J Neurogenet. 2003 Apr-Sep;17(2-3):223-30.PMID: 14668200 [PubMed - indexed for MEDLINE]Related articles

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.

Tan EK, Zhao Y, Puong KY, Law HY, Chan LL, Yew K, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Ng IS.

Neurology. 2004 Jul 27;63(2):362-3.PMID: 15277639 [PubMed - indexed for MEDLINE]Related articles

Fragile X gene premutation in multiple system atrophy.

Garland EM, Vnencak-Jones CL, Biaggioni I, Davis TL, Montine TJ, Robertson D.

J Neurol Sci. 2004 Dec 15;227(1):115-8.PMID: 15546601 [PubMed - indexed for MEDLINE]Related articles