Limprasert P - Search Results

1

Familial transmission of the FMR1 CGG repeat.

Nolin SL, Lewis FA 3rd, Ye LL, Houck GE Jr, Glicksman AE, Limprasert P, Li SY, Zhong N, Ashley AE, Feingold E, Sherman SL, Brown WT. Nolin SL, et al. Among authors: limprasert p. Am J Hum Genet. 1996 Dec;59(6):1252-61. Am J Hum Genet. 1996. PMID: 8940270 Free PMC article.

2

Possible founder effects for FRAXE alleles.

Limprasert P, Zhong N, Currie JR, Brown WT. Limprasert P, et al. Am J Med Genet. 1999 May 28;84(3):286-90. doi: 10.1002/(sici)1096-8628(19990528)84:3<286::aid-ajmg24>3.0.co;2-s. Am J Med Genet. 1999. PMID: 10331609

3

Polymorphism of FXR1 showing lack of association with autism.

Limprasert P, Zhong N, Dobkin C, Brown WT. Limprasert P, et al. Am J Med Genet. 1997 Jul 25;74(4):453-4. Am J Med Genet. 1997. PMID: 9259386 No abstract available.

4

Haplotype analysis at the FRAXA locus in Thai subjects.

Limprasert P, Saechan V, Ruangdaraganon N, Sura T, Vasiknanote P, Jaruratanasirikul S, Brown WT. Limprasert P, et al. Am J Med Genet. 2001 Jan 22;98(3):224-9. Am J Med Genet. 2001. PMID: 11169559

5

The frequency of fragile X syndrome among selected patients at Songklanagarind Hospital during 1991-1996, studied by cytogenetic and molecular methods.

Jinorose U, Vasiknanonte P, Limprasert P, Brown WT, Panich V. Jinorose U, et al. Among authors: limprasert p. Southeast Asian J Trop Med Public Health. 1997;28 Suppl 3:69-74. Southeast Asian J Trop Med Public Health. 1997. PMID: 9640603

6

Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeats.

Limprasert P, Nouri N, Heyman RA, Nopparatana C, Kamonsilp M, Deininger PL, Keats BJ. Limprasert P, et al. Hum Mol Genet. 1996 Feb;5(2):207-13. doi: 10.1093/hmg/5.2.207. Hum Mol Genet. 1996. PMID: 8824876

7

Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene.

Limprasert P, Nouri N, Nopparatana C, Deininger PL, Keats BJ. Limprasert P, et al. Am J Med Genet. 1997 Sep 19;74(5):488-93. doi: 10.1002/(sici)1096-8628(19970919)74:5<488::aid-ajmg6>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9342197

8

A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction.

Elias MH, Ankathil R, Salmi AR, Sudhikaran W, Limprasert P, Zilfalil BA. Elias MH, et al. Among authors: limprasert p. Genet Test Mol Biomarkers. 2011 Jun;15(6):387-93. doi: 10.1089/gtmb.2010.0191. Epub 2011 Feb 17. Genet Test Mol Biomarkers. 2011. PMID: 21329465

9

Screening for FMR1 CGG Repeat Expansion in Thai Patients with Autism Spectrum Disorder.

Hnoonual A, Jankittunpaiboon C, Limprasert P. Hnoonual A, et al. Among authors: limprasert p. Biomed Res Int. 2021 Dec 8;2021:4359308. doi: 10.1155/2021/4359308. eCollection 2021. Biomed Res Int. 2021. PMID: 34926684 Free PMC article.

10

Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier.

Yamada K, Limprasert P, Ratanasukon M, Tengtrisorn S, Yingchareonpukdee J, Vasiknanonte P, Kitaoka T, Ghadami M, Niikawa N, Kishino T. Yamada K, et al. Among authors: limprasert p. Am J Med Genet. 2001 Apr 15;100(1):52-5. doi: 10.1002/1096-8628(20010415)100:1<52::aid-ajmg1214>3.0.co;2-b. Am J Med Genet. 2001. PMID: 11337749

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