409 related articles for article (PubMed ID: 2564838)
21. 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]
22. Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation.
Steinbach P; Barbi G; Baur S; Wiedenmann A
Hum Genet; 1983; 63(4):404-5. PubMed ID: 6683244
[TBL] [Abstract][Full Text] [Related]
23. Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).
Mulley J; Turner G; Bain S; Sutherland GR
Am J Med Genet; 1988; 30(1-2):567-80. PubMed ID: 2902797
[TBL] [Abstract][Full Text] [Related]
24. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Pålsson-Stråe U
Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
[TBL] [Abstract][Full Text] [Related]
25. Two brothers with mental retardation discordant for the fragile-X syndrome.
Van Roy BC; Willems PJ; Vits LJ; Ceulemans BP; Coucke PJ; Van der Auwera BJ; Lormans JA; Dumon JE
Am J Med Genet; 1990 May; 36(1):122-5. PubMed ID: 2333901
[TBL] [Abstract][Full Text] [Related]
26. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
Ventruto V; Stabile M; Gentile G; de Tollis G; Colantuoni M; Sirone P; Perone L; Lonardo F; Della Monica M; Fiore M
Ann Genet; 1986; 29(1):59-61. PubMed ID: 3487280
[TBL] [Abstract][Full Text] [Related]
27. Pulsed-field gradient-gel studies around the fragile site.
Dobkin CS; Brown WT
Am J Med Genet; 1988; 30(1-2):593-600. PubMed ID: 2902798
[TBL] [Abstract][Full Text] [Related]
28. Genetics and expression of the fragile X syndrome.
Brown WT; Jenkins EC; Gross AC; Chan CB; Wisniewski K; Cohen IL; Miezejeski CM
Ups J Med Sci Suppl; 1987; 44():137-54. PubMed ID: 2895523
[TBL] [Abstract][Full Text] [Related]
29. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
Sutherland GR; Baker E
Clin Genet; 1990 Mar; 37(3):167-72. PubMed ID: 2323087
[TBL] [Abstract][Full Text] [Related]
30. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.
Mulligan LM; Phillips MA; Forster-Gibson CJ; Beckett J; Partington MW; Simpson NE; Holden JJ; White BN
Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332
[TBL] [Abstract][Full Text] [Related]
31. [Recombination between the fragile site Xq27 and the gene for coagulation factor IX].
Landoulsi A; de Blois MC; Guérin P; Rethoré MO; Lejeune J; Lucotte G
Ann Genet; 1985; 28(4):201-5. PubMed ID: 3879429
[TBL] [Abstract][Full Text] [Related]
32. Fragile-X mental retardation in a large five-generation family. A clinical and cytogenetic study.
Raimondi E; Lenti C; Romagnoni M; Negri R; Gambini E; Musetti L; De Carli L
Eur Neurol; 1990; 30(1):32-7. PubMed ID: 2298224
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
Vincent A; Dahl N; Oberlé I; Hanauer A; Mandel JL; Malmgren H; Pettersson U
Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
[TBL] [Abstract][Full Text] [Related]
35. Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis.
Nussbaum RL; Airhart SD; Ledbetter DH
Am J Med Genet; 1986; 23(1-2):715-21. PubMed ID: 3456708
[TBL] [Abstract][Full Text] [Related]
36. The fragile X syndrome: variability of expression in carrier females.
Howard-Peebles PN; Brown WT
Am J Med Genet; 1988; 30(1-2):227-30. PubMed ID: 3177448
[TBL] [Abstract][Full Text] [Related]
37. Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation.
Laird CD
Genetics; 1987 Nov; 117(3):587-99. PubMed ID: 3692144
[TBL] [Abstract][Full Text] [Related]
38. Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation.
Wöhrle D; Steinbach P
Hum Genet; 1991 Aug; 87(4):421-4. PubMed ID: 1715307
[TBL] [Abstract][Full Text] [Related]
39. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation.
Pembrey ME; Winter RM; Davies KE
Am J Med Genet; 1985 Aug; 21(4):709-17. PubMed ID: 4040705
[TBL] [Abstract][Full Text] [Related]
40. X-linked mental retardation with the fragile X. A study of 15 families.
Mattei JF; Mattei MG; Aumeras C; Auger M; Giraud F
Hum Genet; 1981; 59(4):281-9. PubMed ID: 7333582
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
