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Results: 1 to 20 of 103

1.

The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients.

Fulchignoni-Lataud MC, Olchwang S, Serre JL.

Eur J Hum Genet. 1997 Mar-Apr;5(2):89-93.

PMID:
9195158
[PubMed - indexed for MEDLINE]
2.

Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range.

Mornet E, Chateau C, Hirst MC, Thepot F, Taillandier A, Cibois O, Serre JL.

Hum Mol Genet. 1996 Jun;5(6):821-5.

PMID:
8776598
[PubMed - indexed for MEDLINE]
Free Article
3.

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]
4.

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]
5.

Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects.

Chen TA, Lu XF, Che PK, Ho WK.

Ann Clin Biochem. 1997 Sep;34 ( Pt 5):517-20.

PMID:
9293305
[PubMed - indexed for MEDLINE]
6.

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
7.

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
[PubMed - indexed for MEDLINE]
Free Article
8.

Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer.

Curia MC, Palmirotta R, Aceto G, Messerini L, Verì MC, Crognale S, Valanzano R, Ficari F, Fracasso P, Stigliano V, Tonelli F, Casale V, Guadagni F, Battista P, Mariani-Costantini R, Cama A.

Cancer Res. 1999 Aug 1;59(15):3570-5.

PMID:
10446963
[PubMed - indexed for MEDLINE]
Free Article
9.
10.

Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice.

Peier AM, Nelson DL.

Genomics. 2002 Oct;80(4):423-32.

PMID:
12376097
[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.

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
[PubMed - indexed for MEDLINE]
Free Article
13.

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ.

Am J Med Genet. 2000 Sep 18;94(3):232-6.

PMID:
10995510
[PubMed - indexed for MEDLINE]
14.

Examination of factors associated with instability of the FMR1 CGG repeat.

Ashley-Koch AE, Robinson H, Glicksman AE, Nolin SL, Schwartz CE, Brown WT, Turner G, Sherman SL.

Am J Hum Genet. 1998 Sep;63(3):776-85.

PMID:
9718348
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Rapid analysis of CGG repeat length in the FMR1 gene.

Poon PM, Zhao Z, Wu XQ, Ni YX, Pang CP.

Clin Chem Lab Med. 2000 Sep;38(9):935-8.

PMID:
11097353
[PubMed - indexed for MEDLINE]
16.

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

Eichler EE, Hammond HA, Macpherson JN, Ward PA, Nelson DL.

Hum Mol Genet. 1995 Dec;4(12):2199-208.

PMID:
8634688
[PubMed - indexed for MEDLINE]
17.

Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.

Brown TC, Tarleton JC, Go RC, Longshore JW, Descartes M.

Am J Med Genet. 1997 Dec 31;73(4):447-55.

PMID:
9415473
[PubMed - indexed for MEDLINE]
18.

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.

Grasso M, Faravelli F, Lo Nigro C, Chiurazzi P, Sperandeo MP, Argusti A, Pomponi MG, Lecora M, Sebastio GF, Perroni L, Andria G, Neri G, Bricarelli FD.

Am J Med Genet. 1999 Jul 30;85(3):311-6.

PMID:
10398249
[PubMed - indexed for MEDLINE]
19.

Pilot fragile X screening in normal population of Taiwan.

Tzeng CC, Cho WC, Kuo PL, Chen RM.

Diagn Mol Pathol. 1999 Sep;8(3):152-6.

PMID:
10565687
[PubMed - indexed for MEDLINE]
20.

Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese.

Wang YC, Li C, Lin ML, Lin WH, Li SY.

J Formos Med Assoc. 2000 May;99(5):402-7.

PMID:
10870330
[PubMed - indexed for MEDLINE]

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