87 related articles for article (PubMed ID: 11281215)
1. Allelic association in the FRAX region.
Ennis S; Collins A; Murray A; Macpherson JN; Morton NE
Ann Hum Genet; 2000 Nov; 64(Pt 6):513-8. PubMed ID: 11281215
[TBL] [Abstract][Full Text] [Related]
2. Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?
Zhong N; Ye L; Dobkin C; Brown WT
Am J Med Genet; 1994 Jul; 51(4):405-11. PubMed ID: 7943008
[TBL] [Abstract][Full Text] [Related]
3. Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.
Chiurazzi P; Genuardi M; Kozak L; Giovannucci-Uzielli ML; Bussani C; Dagna-Bricarelli F; Grasso M; Perroni L; Sebastio G; Sperandeo MP; Oostra BA; Neri G
Am J Med Genet; 1996 Jul; 64(1):209-15. PubMed ID: 8826478
[TBL] [Abstract][Full Text] [Related]
4. Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect?
Ennis S; Murray A; Morton NE
Hum Mutat; 2001; 18(1):61-9. PubMed ID: 11438994
[TBL] [Abstract][Full Text] [Related]
5. Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.
Oudet C; Mornet E; Serre JL; Thomas F; Lentes-Zengerling S; Kretz C; Deluchat C; Tejada I; Boué J; Boué A
Am J Hum Genet; 1993 Feb; 52(2):297-304. PubMed ID: 8094266
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. The optimal measure of allelic association.
Morton NE; Zhang W; Taillon-Miller P; Ennis S; Kwok PY; Collins A
Proc Natl Acad Sci U S A; 2001 Apr; 98(9):5217-21. PubMed ID: 11309498
[TBL] [Abstract][Full Text] [Related]
9. Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate.
Arinami T; Asano M; Kobayashi K; Yanagi H; Hamaguchi H
Hum Genet; 1993 Nov; 92(5):431-6. PubMed ID: 8244331
[TBL] [Abstract][Full Text] [Related]
10. A high-density SNP map for the FRAX region of the X chromosome. Single-nucleotide polymorphisms.
Brightwell G; Wycherley R; Potts G; Waghorn A
J Hum Genet; 2002; 47(11):567-75. PubMed ID: 12436192
[TBL] [Abstract][Full Text] [Related]
11. Allelic association with SNPs: metrics, populations, and the linkage disequilibrium map.
Collins A; Ennis S; Taillon-Miller P; Kwok PY; Morton NE
Hum Mutat; 2001 Apr; 17(4):255-62. PubMed ID: 11295822
[TBL] [Abstract][Full Text] [Related]
12. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.
Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; Constantinou-Deltas CD; Pagoulatos G
Am J Med Genet; 1996 Jul; 64(1):234-8. PubMed ID: 8826482
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 8852655
[TBL] [Abstract][Full Text] [Related]
14. Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.
Murray A; Youings S; Dennis N; Latsky L; Linehan P; McKechnie N; Macpherson J; Pound M; Jacobs P
Hum Mol Genet; 1996 Jun; 5(6):727-35. PubMed ID: 8776586
[TBL] [Abstract][Full Text] [Related]
15. Comparative informativeness for linkage of multiple SNPs and single microsatellites.
Lindholm E; Hodge SE; Greenberg DA
Hum Hered; 2004; 58(3-4):164-70. PubMed ID: 15812173
[TBL] [Abstract][Full Text] [Related]
16. FMR1 haplotype analyses among Indians: a weak founder effect and other findings.
Sharma D; Gupta M; Thelma BK
Hum Genet; 2003 Mar; 112(3):262-71. PubMed ID: 12596051
[TBL] [Abstract][Full Text] [Related]
17. Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests.
Kieffer E; Nicod JC; Gardes N; Kastner C; Becker N; Celebi C; Pirrello O; Rongières C; Koscinski I; Gosset P; Moutou C
Eur J Hum Genet; 2016 Feb; 24(2):221-7. PubMed ID: 25966634
[TBL] [Abstract][Full Text] [Related]
18. 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; 84(3):204-7. PubMed ID: 10331592
[TBL] [Abstract][Full Text] [Related]
19. 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; 64(1):226-33. PubMed ID: 8826481
[TBL] [Abstract][Full Text] [Related]
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; 6(5):518-22. PubMed ID: 9801877
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
