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Results: 1 to 20 of 103

1.

Genetic diversity at the FMR1 locus in Mexican population.

Rosales-Reynoso MA, Mendoza-Carrera F, Troyo-Sanromán R, Medina C, Barros-Núñez P.

Arch Med Res. 2005 Jul-Aug;36(4):412-7.

PMID:
15950084
[PubMed - indexed for MEDLINE]
2.

Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1.

Stöger R, Kajimura TM, Brown WT, Laird CD.

Hum Mol Genet. 1997 Oct;6(11):1791-801.

PMID:
9302255
[PubMed - indexed for MEDLINE]
Free Article
3.

Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara.

Barros-Núñez P, Rosales-Reynoso MA, Sandoval L, Romero-Espinoza P, Troyo-Sanromán R, Ibarra B.

Am J Hum Biol. 2008 May-Jun;20(3):259-63. doi: 10.1002/ajhb.20705.

PMID:
18172867
[PubMed - indexed for MEDLINE]
4.

A methylation PCR approach for detection of fragile X syndrome.

Panagopoulos I, Lassen C, Kristoffersson U, Aman P.

Hum Mutat. 1999;14(1):71-9.

PMID:
10447261
[PubMed - indexed for MEDLINE]
5.

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.

Meijer H, de Graaff E, Merckx DM, Jongbloed RJ, de Die-Smulders CE, Engelen JJ, Fryns JP, Curfs PM, Oostra BA.

Hum Mol Genet. 1994 Apr;3(4):615-20.

PMID:
8069307
[PubMed - indexed for MEDLINE]
6.

Haplotype study of intermediate-length alleles at the fragile X (FMR1) gene: ATL1, FMRb, and microsatellite haplotypes differ from those found in common-size FMR1 alleles.

Curlis Y, Zhang C, Holden JJ, Loesch PK, Mitchell RJ.

Hum Biol. 2005 Feb;77(1):137-51.

PMID:
16114822
[PubMed - indexed for MEDLINE]
7.

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.

Snow K, Doud LK, Hagerman R, Pergolizzi RG, Erster SH, Thibodeau SN.

Am J Hum Genet. 1993 Dec;53(6):1217-28.

PMID:
7902673
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion.

Milà M, Castellví-Bel S, Giné R, Vazquez C, Badenas C, Sánchez A, Estivill X.

Hum Genet. 1996 Oct;98(4):419-21.

PMID:
8792815
[PubMed - indexed for MEDLINE]
9.

FMR1 in global populations.

Kunst CB, Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST.

Am J Hum Genet. 1996 Mar;58(3):513-22.

PMID:
8644711
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.

Sharma D, Gupta M, Thelma BK.

Genet Epidemiol. 2001 Jan;20(1):129-144.

PMID:
11119302
[PubMed - indexed for MEDLINE]
11.

Transcription of the FMR1 gene in individuals with fragile X syndrome.

Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ.

Am J Med Genet. 2000 Fall;97(3):195-203.

PMID:
11449488
[PubMed - indexed for MEDLINE]
12.

Rare variants in the promoter of the fragile X syndrome gene (FMR1).

Milà M, Castellví-Bel S, Sánchez A, Barceló A, Badenas C, Mallolas J, Estivill X.

Mol Cell Probes. 2000 Apr;14(2):115-9.

PMID:
10799273
[PubMed - indexed for MEDLINE]
13.

Allele distribution at the FMR1 locus in the general Chinese population.

Chiang SC, Lee YM, Wang TR, Hwu WL.

Clin Genet. 1999 May;55(5):352-5.

PMID:
10422806
[PubMed - indexed for MEDLINE]
14.

Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.

Patsalis PC, Sismani C, Stylianou S, Ioannou P, Joseph G, Manoli P, Holden JJ, Hettinger JA.

Am J Med Genet. 1999 May 28;84(3):217-20.

PMID:
10331595
[PubMed - indexed for MEDLINE]
15.

Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals.

Genç B, Müller-Hartmann H, Zeschnigk M, Deissler H, Schmitz B, Majewski F, von Gontard A, Doerfler W.

Nucleic Acids Res. 2000 May 15;28(10):2141-52.

PMID:
10773084
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Mosaicism for full mutation and normal-sized allele of the FMR1 gene: a new case.

Orrico A, Galli L, Dotti MT, Plewnia K, Censini S, Federico A.

Am J Med Genet. 1998 Jul 24;78(4):341-4.

PMID:
9714436
[PubMed - indexed for MEDLINE]
17.

Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome.

Milewski M, Zygulska M, Bal J, Deelen WH, Obersztyn E, Bocian E, Halley DJ, Horst J, Mazurczak T.

Acta Biochim Pol. 1996;43(2):383-8.

PMID:
8862184
[PubMed - indexed for MEDLINE]
Free Article
18.

Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.

Garcia Arocena D, Breece KE, Hagerman PJ.

Hum Genet. 2003 Oct;113(5):371-6. Epub 2003 Aug 7.

PMID:
12905066
[PubMed - indexed for MEDLINE]
19.

Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression.

Grønskov K, Hjalgrim H, Bjerager MO, Brøndum-Nielsen K.

Am J Hum Genet. 1997 Oct;61(4):961-7.

PMID:
9382110
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Methylation analysis of CGG sites in the CpG island of the human FMR1 gene.

Hansen RS, Gartler SM, Scott CR, Chen SH, Laird CD.

Hum Mol Genet. 1992 Nov;1(8):571-8.

PMID:
1301165
[PubMed - indexed for MEDLINE]
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