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Items: 1 to 20 of 138

1.

FRAXAC1 and DXS548 polymorphisms in the Chinese population.

Poon PM, Pang CP, Chen QL, Zhong N, Lai KY, Lau CH, Wong CK, Brown WT.

Am J Med Genet. 1999 May 28;84(3):208-13.

PMID:
10331593
2.

Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.

Jara L, Aspillaga M, Avendaño I, Obreque V, Blanco R, Valenzuela CY.

Am J Med Genet. 1998 Jan 23;75(3):277-82.

PMID:
9475597
3.

Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.

Larsen LA, Vuust J, Nystad M, Evseeva I, Van Ghelue M, Tranebjaerg L.

Eur J Hum Genet. 2001 Sep;9(9):724-7.

5.

Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.

Pekarík V, Blazková M, Kozák L.

Am J Med Genet. 1999 May 28;84(3):214-6.

PMID:
10331594
6.

Fragile X founder effects and new mutations in Finland.

Zhong N, Kajanoja E, Smits B, Pietrofesa J, Curley D, Wang D, Ju W, Nolin S, Dobkin C, Ryynänen M, Brown WT.

Am J Med Genet. 1996 Jul 12;64(1):226-33.

PMID:
8826481
7.

Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations.

Mingroni-Netto RC, Angeli CB, Auricchio MT, Leal-Mesquita ER, Ribeiro-dos-Santos AK, Ferrari I, Hutz MH, Salzano FM, Hill K, Hurtado AM, Vianna-Morgante AM.

Am J Med Genet. 2002 Aug 15;111(3):243-52.

PMID:
12210320
8.

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL.

Hum Mol Genet. 1996 Mar;5(3):319-30.

PMID:
8852655
9.

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
10.

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

Patsalis PC, Sismani C, Hettinger JA, Boumba I, Georgiou I, Stylianidou G, Anastasiadou V, Koukoulli R, Pagoulatos G, Syrrou M.

Am J Med Genet. 1999 May 28;84(3):184-90.

PMID:
10331587
11.

Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.

Zhong N, Ju W, Xu W, Ye L, Shen Y, Wu G, Chen SH, Jin R, Hu XF, Yang A, Liu X, Poon P, Pang C, Zheng Y, Song L, Zhao P, Fu B, Gu H, Brown WT.

Am J Med Genet. 1999 May 28;84(3):191-4.

PMID:
10331588
12.

Haplotype analysis at the FRAXA locus in an Indian population.

Chakraborty SS, Mondal BC, Das S, Das K, Dasgupta UB.

Am J Med Genet A. 2008 Aug 1;146A(15):1980-5. doi: 10.1002/ajmg.a.32108.

PMID:
18627041
13.

Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.

Larsen LA, Armstrong JS, Grønskov K, Hjalgrim H, Macpherson JN, Brøndum-Nielsen K, Hasholt L, Nørgaard-Pedersen B, Vuust J.

Am J Med Genet. 2000 Jul 17;93(2):99-106.

PMID:
10869110
14.

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
15.

AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations.

Angeli CB, Capelli LP, Auricchio MT, Leal-Mesquita ER, Ribeiro-dos-Santos AK, Ferrari I, Oliveira SF, Klautau-Guimarães Mde N, Vianna-Morgante AM, Mingroni-Netto RC.

Am J Med Genet A. 2005 Jan 15;132A(2):210-4. No abstract available. Erratum in: Am J Med Genet A. 2005 Jul 1;136(1):112.

PMID:
15551304
16.

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

Zhong N, Liu X, Gou S, Houck GE Jr, Li S, Dobkin C, Brown WT.

Am J Med Genet. 1994 Jul 15;51(4):417-22.

PMID:
7943010
17.

Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia.

Larsen LA, Armstrong JS, Grønskov K, Hjalgrim H, Brøndum-Nielsen K, Hasholt L, Nørgaard-Pedersen B, Vuust J.

Eur J Hum Genet. 1999 Oct-Nov;7(7):771-7.

18.

Response to Poon et al.-"FRAXAC1 and DXS548 polymorphisms in the Chinese population".

Pandey UB.

Am J Med Genet A. 2003 Oct 1;122A(2):186. No abstract available.

PMID:
12955775
19.

DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population.

Mingroni-Netto RC, Costa SS, Angeli CB, Vianna-Morgante AM.

Am J Med Genet. 1999 May 28;84(3):204-7.

PMID:
10331592
20.

Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype.

Peixoto A, dos Santos MR, Seruca R, Amorim A, Castedo S.

Eur J Hum Genet. 1998 Sep-Oct;6(5):518-22.

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