275 related articles for article (PubMed ID: 10409756)
41. Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.
Dombrowski C; Lévesque S; Morel ML; Rouillard P; Morgan K; Rousseau F
Hum Mol Genet; 2002 Feb; 11(4):371-8. PubMed ID: 11854169
[TBL] [Abstract][Full Text] [Related]
42. Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice.
Lavedan C; Grabczyk E; Usdin K; Nussbaum RL
Genomics; 1998 Jun; 50(2):229-40. PubMed ID: 9653650
[TBL] [Abstract][Full Text] [Related]
43. The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing.
Kunst CB; Leeflang EP; Iber JC; Arnheim N; Warren ST
J Med Genet; 1997 Aug; 34(8):627-31. PubMed ID: 9279752
[TBL] [Abstract][Full Text] [Related]
44. Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.
Gurling HM; Bolton PF; Vincent J; Melmer G; Rutter M
Hum Hered; 1997; 47(5):254-62. PubMed ID: 9358013
[TBL] [Abstract][Full Text] [Related]
45. 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. PubMed ID: 10870330
[TBL] [Abstract][Full Text] [Related]
46. 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. PubMed ID: 9811938
[TBL] [Abstract][Full Text] [Related]
47. 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; 85(3):311-6. PubMed ID: 10398249
[TBL] [Abstract][Full Text] [Related]
48. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
[TBL] [Abstract][Full Text] [Related]
49. 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. PubMed ID: 8776598
[TBL] [Abstract][Full Text] [Related]
50. Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients.
de Graaff E; Rouillard P; Willems PJ; Smits AP; Rousseau F; Oostra BA
Hum Mol Genet; 1995 Jan; 4(1):45-9. PubMed ID: 7711733
[TBL] [Abstract][Full Text] [Related]
51. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; Ng V; Chitnis X; McGuire P; Suckling J; Davies KE; Hagerman RJ; Hagerman PJ; Murphy KC; Murphy DG
Brain; 2004 Dec; 127(Pt 12):2672-81. PubMed ID: 15483045
[TBL] [Abstract][Full Text] [Related]
52. 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. PubMed ID: 1301165
[TBL] [Abstract][Full Text] [Related]
53. Fragile X syndrome.
Chakrabarti L; Davies KE
Curr Opin Neurol; 1997 Apr; 10(2):142-7. PubMed ID: 9146995
[TBL] [Abstract][Full Text] [Related]
54. 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; 5(2):89-93. PubMed ID: 9195158
[TBL] [Abstract][Full Text] [Related]
55. Precursor arrays for triplet repeat expansion at the fragile X locus.
Hirst MC; Grewal PK; Davies KE
Hum Mol Genet; 1994 Sep; 3(9):1553-60. PubMed ID: 7833910
[TBL] [Abstract][Full Text] [Related]
56. 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. PubMed ID: 10447261
[TBL] [Abstract][Full Text] [Related]
57. Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor.
de Graaff E; Willemsen R; Zhong N; de Die-Smulders CE; Brown WT; Freling G; Oostra B
Am J Hum Genet; 1995 Sep; 57(3):609-18. PubMed ID: 7668289
[TBL] [Abstract][Full Text] [Related]
58. Use of human-derived stem cells to create a novel, in vitro model designed to explore FMR1 CGG repeat instability amongst female premutation carriers.
Gustin SLF; Wang G; Baker VM; Latham G; Sebastiano V
J Assist Reprod Genet; 2018 Aug; 35(8):1443-1455. PubMed ID: 29926373
[TBL] [Abstract][Full Text] [Related]
59. Double-strand break repair can lead to high frequencies of deletions within short CAG/CTG trinucleotide repeats.
Richard GF; Dujon B; Haber JE
Mol Gen Genet; 1999 Jun; 261(4-5):871-82. PubMed ID: 10394925
[TBL] [Abstract][Full Text] [Related]
60. A fragile X case with an amplification/deletion mosaic pattern.
García Arocena D; de Diego Y; Oostra BA; Willemsen R; Mirta Rodriguez M
Hum Genet; 2000 Mar; 106(3):366-9. PubMed ID: 10798369
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]