174 related articles for article (PubMed ID: 12210320)
1. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations.
Mingroni-Netto RC; Angeli CB; Auricchio MT; Leal-Mesquita ER; Ribeiro-dos-Santos AK; Ferrari I; Hutz MH; Salzano FM; Hill K; Hurtado AM; Vianna-Morgante AM
Am J Med Genet; 2002 Aug; 111(3):243-52. PubMed ID: 12210320
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 16114822
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 11571563
[TBL] [Abstract][Full Text] [Related]
4. FRAXAC1 and DXS548 polymorphisms in the Chinese population.
Poon PM; Pang CP; Chen QL; Zhong N; Lai KY; Lau CH; Wong CK; Brown WT
Am J Med Genet; 1999 May; 84(3):208-13. PubMed ID: 10331593
[TBL] [Abstract][Full Text] [Related]
5. AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations.
Angeli CB; Capelli LP; Auricchio MT; Leal-Mesquita ER; Ribeiro-dos-Santos AK; Ferrari I; Oliveira SF; Klautau-Guimarães Mde N; Vianna-Morgante AM; Mingroni-Netto RC
Am J Med Genet A; 2005 Jan; 132A(2):210-4. PubMed ID: 15551304
[No Abstract] [Full Text] [Related]
6. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.
Jara L; Aspillaga M; Avendaño I; Obreque V; Blanco R; Valenzuela CY
Am J Med Genet; 1998 Jan; 75(3):277-82. PubMed ID: 9475597
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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. PubMed ID: 10677308
[TBL] [Abstract][Full Text] [Related]
9. Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population.
Chiurazzi P; Destro-Bisol G; Genuardi M; Oostra BA; Spedini G; Neri G
Am J Med Genet; 1996 Jul; 64(1):216-9. PubMed ID: 8826479
[TBL] [Abstract][Full Text] [Related]
10. Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.
Zhong N; Liu X; Gou S; Houck GE; Li S; Dobkin C; Brown WT
Am J Med Genet; 1994 Jul; 51(4):417-22. PubMed ID: 7943010
[TBL] [Abstract][Full Text] [Related]
11. FMR1 CGG repeat distribution and linked microsatellite-SNP haplotypes in normal Mexican Mestizo and indigenous populations.
Felix-López XA; Argüello-García R; Cerda-Flores RM; Peñaloza-Espinoza RI; Buentello-Malo L; Estrada-Mena FJ; Ramos-Kuri M; Gómez FS; Arenas-Aranda DJ
Hum Biol; 2006 Oct; 78(5):579-98. PubMed ID: 17506288
[TBL] [Abstract][Full Text] [Related]
12. Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.
Tzeng CC; Tsai LP; Hwu WL; Lin SJ; Chao MC; Jong YJ; Chu SY; Chao WC; Lu CL
Am J Med Genet A; 2005 Feb; 133A(1):37-43. PubMed ID: 15637705
[TBL] [Abstract][Full Text] [Related]
13. 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; 7(7):771-7. PubMed ID: 10573009
[TBL] [Abstract][Full Text] [Related]
14. Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.
Pekarík V; Blazková M; Kozák L
Am J Med Genet; 1999 May; 84(3):214-6. PubMed ID: 10331594
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.
Peprah EK; Allen EG; Williams SM; Woodard LM; Sherman SL
Ann Hum Genet; 2010 Jul; 74(4):316-25. PubMed ID: 20597902
[TBL] [Abstract][Full Text] [Related]
17. Haplotype Analysis of DXS548 and FRAXAC1 Microsatellite Loci in Iranian Patients with Fragile X Syndrome.
Aleyasin SA; Salamat F; Mirakhori M
Iran J Child Neurol; 2018; 12(1):36-46. PubMed ID: 29379561
[TBL] [Abstract][Full Text] [Related]
18. The identification of a (CGG)6AGG insertion within the CGG repeat of the FMR1 gene in Asians.
Chen SH; Schoof JM; Buroker NE; Scott CR
Hum Genet; 1997 Jun; 99(6):793-5. PubMed ID: 9187675
[TBL] [Abstract][Full Text] [Related]
19. Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population.
Huang W; Xia Q; Luo S; He H; Zhu T; Du Q; Duan R
Mol Genet Genomic Med; 2015 May; 3(3):172-81. PubMed ID: 26029703
[TBL] [Abstract][Full Text] [Related]
20. 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; 93(2):99-106. PubMed ID: 10869110
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
