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Items: 1 to 20 of 83

1.

Single nucleotide polymorphism and FMR1 CGG repeat instability in two Basque valleys.

Barasoain M, Barrenetxea G, Ortiz-Lastra E, González J, Huerta I, Télez M, Ramírez JM, Domínguez A, Gurtubay P, Criado B, Arrieta I.

Ann Hum Genet. 2012 Mar;76(2):110-20. doi: 10.1111/j.1469-1809.2011.00696.x. Epub 2012 Jan 2.

2.

The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys.

Arrieta I, Peñagarikano O, Télez M, Ortega B, Flores P, Criado B, Veiga I, Peixoto AL, Lostao CM.

Heredity (Edinb). 2003 Mar;90(3):206-11.

4.

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST.

Hum Mol Genet. 1998 Nov;7(12):1935-46.

PMID:
9811938
5.

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
6.

Fragile X gene stability in Basque Valleys: prevalence of premutation and intermediate alleles.

Arrieta I, Télez M, Huerta I, Flores P, Criado B, Ramírez JM, Barasoain M, Gónzalez AJ.

Hum Biol. 2008 Dec;80(6):593-600.

PMID:
19728537
7.

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
8.

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.

9.

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
10.

FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.

Zhou Y, Tang K, Law HY, Ng IS, Lee CG, Chong SS.

Ann Hum Genet. 2006 Nov;70(Pt 6):784-96.

11.

Analysis of the Fragile X Trinucleotide Repeat in Basques: Association of Premutation and Intermediate Sizes, Anchoring AGGs and Linked Microsatellites with Unstable Alleles.

Arrieta MI, Ramírez JM, Télez M, Flores P, Criado B, Barasoain M, Huerta I, González AJ.

Curr Genomics. 2008 May;9(3):191-9. doi: 10.2174/138920208784340722.

12.

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
13.

A new insight into fragile X syndrome among Basque population.

Peñagarikano O, Gil A, Télez M, Ortega B, Flores P, Veiga I, Peixoto A, Criado B, Arrieta I.

Am J Med Genet A. 2004 Jul 30;128A(3):250-5.

PMID:
15216545
14.

Stability of the FMR1 CGG repeat in a Basque sample.

Arrieta I, Gil A, Nuñez T, Telez M, Martinez B, Criado B, Lostao C.

Hum Biol. 1999 Feb;71(1):55-68.

PMID:
9972098
15.

Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.

Crawford DC, Zhang F, Wilson B, Warren ST, Sherman SL.

Hum Mol Genet. 2000 Jul 22;9(12):1759-69.

PMID:
10915764
16.

Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?

Maia N, Loureiro JR, Oliveira B, Marques I, Santos R, Jorge P, Martins S.

J Hum Genet. 2017 Feb;62(2):269-275. doi: 10.1038/jhg.2016.122. Epub 2016 Oct 27.

PMID:
27784894
18.

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, Sherman SL.

Am J Hum Genet. 2000 Feb;66(2):480-93.

19.

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.

20.

Instability of a (CGG)98 repeat in the Fmr1 promoter.

Bontekoe CJ, Bakker CE, Nieuwenhuizen IM, van der Linde H, Lans H, de Lange D, Hirst MC, Oostra BA.

Hum Mol Genet. 2001 Aug 1;10(16):1693-9.

PMID:
11487573

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