166 related articles for article (PubMed ID: 8105267)
1. Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndrome.
Wang Q; Green E; Barnicoat A; Garrett D; Mullarkey M; Bobrow M; Mathew CG
Lancet; 1993 Oct; 342(8878):1025-6. PubMed ID: 8105267
[TBL] [Abstract][Full Text] [Related]
2. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.
Knight SJ; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; Mueller RF; Hurst J; Paterson J; Yates JR; Dow DJ; Davies KE
Am J Hum Genet; 1996 May; 58(5):906-13. PubMed ID: 8651274
[TBL] [Abstract][Full Text] [Related]
3. Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.
Ramos FJ; Emanuel BS; Spinner NB
Am J Med Genet; 1992 Apr; 42(6):835-8. PubMed ID: 1532475
[TBL] [Abstract][Full Text] [Related]
4. Characterisation of a new rare fragile site easily confused with the fragile X.
Sutherland GR; Baker E
Hum Mol Genet; 1992 May; 1(2):111-3. PubMed ID: 1301146
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. The fragile X syndrome.
de Vries BB; Halley DJ; Oostra BA; Niermeijer MF
J Med Genet; 1998 Jul; 35(7):579-89. PubMed ID: 9678703
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Human chromosome fragility.
Lukusa T; Fryns JP
Biochim Biophys Acta; 2008 Jan; 1779(1):3-16. PubMed ID: 18078840
[TBL] [Abstract][Full Text] [Related]
12. Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.
Flynn GA; Hirst MC; Knight SJ; Macpherson JN; Barber JC; Flannery AV; Davies KE; Buckle VJ
J Med Genet; 1993 Feb; 30(2):97-100. PubMed ID: 8445629
[TBL] [Abstract][Full Text] [Related]
13. The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
Ritchie RJ; Knight SJ; Hirst MC; Grewal PK; Bobrow M; Cross GS; Davies KE
Hum Mol Genet; 1994 Dec; 3(12):2115-21. PubMed ID: 7881407
[TBL] [Abstract][Full Text] [Related]
14. FRAXA and FRAXE: the results of a five year survey.
Youings SA; Murray A; Dennis N; Ennis S; Lewis C; McKechnie N; Pound M; Sharrock A; Jacobs P
J Med Genet; 2000 Jun; 37(6):415-21. PubMed ID: 10851251
[TBL] [Abstract][Full Text] [Related]
15. Chromosome fragility at FRAXA in human cleavage stage embryos at risk for fragile X syndrome.
Verdyck P; Berckmoes V; De Vos A; Verpoest W; Liebaers I; Bonduelle M; De Rycke M
Am J Med Genet A; 2015 Oct; 167A(10):2306-13. PubMed ID: 25953684
[TBL] [Abstract][Full Text] [Related]
16. [FRAXE mental retardation].
Yamagata T
Nihon Rinsho; 1999 Apr; 57(4):955-9. PubMed ID: 10222796
[TBL] [Abstract][Full Text] [Related]
17. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.
Jenkins EC; Genovese MJ; Duncan CJ; Gu H; Stark-Houck SL; Lele K; Li SY; Krawczun MS
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):136-41. PubMed ID: 1605182
[TBL] [Abstract][Full Text] [Related]
18. Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.
Hamel BC; Smits AP; de Graaff E; Smeets DF; Schoute F; Eussen BH; Knight SJ; Davies KE; Assman-Hulsmans CF; Oostra BA
Am J Hum Genet; 1994 Nov; 55(5):923-31. PubMed ID: 7977354
[TBL] [Abstract][Full Text] [Related]
19. Experience with direct molecular diagnosis of fragile X.
Mulley JC; Yu S; Gedeon AK; Donnelly A; Turner G; Loesch D; Chapman CJ; Gardner RJ; Richards RI; Sutherland GR
J Med Genet; 1992 Jun; 29(6):368-74. PubMed ID: 1619631
[TBL] [Abstract][Full Text] [Related]
20. FRAXE expansion is not a common etiological factor among developmentally delayed males.
Allingham-Hawkins DJ; Ray PN
Am J Hum Genet; 1995 Jul; 57(1):72-6. PubMed ID: 7541938
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]