163 related articles for article (PubMed ID: 8776586)
21. Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.
Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; Romac S
J Neurogenet; 2003; 17(2-3):223-30. PubMed ID: 14668200
[TBL] [Abstract][Full Text] [Related]
22. Clinical, cytogenetic, and molecular analysis of three families with FRAXE.
Barnicoat AJ; Wang Q; Turk J; Green E; Mathew CG; Flynn G; Buckle V; Hirst M; Davies K; Bobrow M
J Med Genet; 1997 Jan; 34(1):13-7. PubMed ID: 9032643
[TBL] [Abstract][Full Text] [Related]
23. FRAXE mutation in mentally retarded patients using the OxE18 probe.
Mulatinho MV; Llerena JC; Pimentel MM
Int J Mol Med; 2000 Jan; 5(1):67-9. PubMed ID: 10601577
[TBL] [Abstract][Full Text] [Related]
24. Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.
Biancalana V; Taine L; Bouix JC; Finck S; Chauvin A; De Verneuil H; Knight SJ; Stoll C; Lacombe D; Mandel JL
Am J Hum Genet; 1996 Oct; 59(4):847-54. PubMed ID: 8808600
[TBL] [Abstract][Full Text] [Related]
25. Stability and haplotype analysis of the FRAXE region.
Murray A; Ennis S; Youings SA; Sharrock AJ; Lewis C; Pound MC; Macpherson JN; Dennis NR; Morton NE; Jacobs PA
Eur J Hum Genet; 2000 Aug; 8(8):583-9. PubMed ID: 10951520
[TBL] [Abstract][Full Text] [Related]
26. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL
Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164
[TBL] [Abstract][Full Text] [Related]
27. Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spots.
Dawson AJ; Chodirker BN; Chudley AE
Biochem Mol Med; 1995 Oct; 56(1):63-9. PubMed ID: 8593539
[TBL] [Abstract][Full Text] [Related]
28. Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.
Crawford DC; Meadows KL; Newman JL; Taft LF; Pettay DL; Gold LB; Hersey SJ; Hinkle EF; Stanfield ML; Holmgreen P; Yeargin-Allsopp M; Boyle C; Sherman SL
Am J Hum Genet; 1999 Feb; 64(2):495-507. PubMed ID: 9973286
[TBL] [Abstract][Full Text] [Related]
29. A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs.
Strelnikov V; Nemtsova M; Chesnokova G; Kuleshov N; Zaletayev D
Hum Mutat; 1999; 13(2):166-9. PubMed ID: 10094554
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. [FRAXE mental retardation].
Yamagata T
Nihon Rinsho; 1999 Apr; 57(4):955-9. PubMed ID: 10222796
[TBL] [Abstract][Full Text] [Related]
32. 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; 28(10):2141-52. PubMed ID: 10773084
[TBL] [Abstract][Full Text] [Related]
33. Clinical, cytogenetic, and molecular description of a FRAXE French family.
Lesca G; Biancalana V; Brunel MJ; Quack B; Calender A; Lespinasse J
Psychiatr Genet; 2003 Mar; 13(1):43-6. PubMed ID: 12605100
[TBL] [Abstract][Full Text] [Related]
34. The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
Hirst MC; Barnicoat A; Flynn G; Wang Q; Daker M; Buckle VJ; Davies KE; Bobrow M
Hum Mol Genet; 1993 Feb; 2(2):197-200. PubMed ID: 8499907
[TBL] [Abstract][Full Text] [Related]
35. Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXE.
Subramanian PS; Nelson DL; Chinault AC
Am J Hum Genet; 1996 Aug; 59(2):407-16. PubMed ID: 8755928
[TBL] [Abstract][Full Text] [Related]
36. Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.
Holden JJ; Wing M; Chalifoux M; Julien-Inalsingh C; Schutz C; Robinson P; Szatmari P; White BN
Am J Med Genet; 1996 Aug; 64(2):399-403. PubMed ID: 8844091
[TBL] [Abstract][Full Text] [Related]
37. Haplotype analysis at the FRAXA locus in Thai subjects.
Limprasert P; Saechan V; Ruangdaraganon N; Sura T; Vasiknanote P; Jaruratanasirikul S; Brown WT
Am J Med Genet; 2001 Jan; 98(3):224-9. PubMed ID: 11169559
[TBL] [Abstract][Full Text] [Related]
38. Unexpected Associations between the Number of FRAXE Repeats in Boys and Evidence of Diabetes in Their Mothers and Maternal Grandmothers.
Golding J; Clark R; Gregory S; Ellis G; Suderman M; Iles-Caven Y; Pembrey ME
OBM Genet; 2021 Oct; 5(4):15. PubMed ID: 35494534
[TBL] [Abstract][Full Text] [Related]
39. Microdeletions in FMR2 may be a significant cause of premature ovarian failure.
Murray A; Webb J; Dennis N; Conway G; Morton N
J Med Genet; 1999 Oct; 36(10):767-70. PubMed ID: 10528856
[TBL] [Abstract][Full Text] [Related]
40. A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci.
Wang Q; Green E; Bobrow M; Mathew CG
J Med Genet; 1995 Mar; 32(3):170-3. PubMed ID: 7783163
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
