494 related articles for article (PubMed ID: 2895524)
1. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
Mulley JC; Gedeon AK; Thorn KA; Bates LJ; Sutherland GR
Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
[TBL] [Abstract][Full Text] [Related]
4. [Mental retardation linked to fragility of chromosome X: current knowledge].
Mattei JF; Mattei MG; Auger M; Giraud F
J Genet Hum; 1984 Jul; 32(3):167-92. PubMed ID: 6237176
[TBL] [Abstract][Full Text] [Related]
5. The fragile X syndrome.
Brown WT
Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
[TBL] [Abstract][Full Text] [Related]
6. [Fragile X syndrome: current knowledge].
Pellissier MC; Voelckel MA; Mattei JF
Pediatrie; 1992; 47(11):743-50. PubMed ID: 1364151
[TBL] [Abstract][Full Text] [Related]
7. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
Fishburn J; Turner G; Daniel A; Brookwell R
Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625
[TBL] [Abstract][Full Text] [Related]
8. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
Rocchi M; Archidiacono N; Filippi G
J Genet Hum; 1987 Dec; 35(5):351-79. PubMed ID: 3437265
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
Soudek D; Partington MW; Lawson JS
Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation.
Rousseau F; Heitz D; Biancalana V; Blumenfeld S; Kretz C; Boué J; Tommerup N; Van Der Hagen C; DeLozier-Blanchet C; Croquette MF
N Engl J Med; 1991 Dec; 325(24):1673-81. PubMed ID: 1944467
[TBL] [Abstract][Full Text] [Related]
13. Fragile X-linked mental retardation and the difficulties of reverse genetics.
Jordan BR
Bioessays; 1991 May; 13(5):243-51. PubMed ID: 1679986
[TBL] [Abstract][Full Text] [Related]
14. Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes.
Goonewardena P; Gustavson KH; Holmgren G; Tolun A; Chotai J; Johnsen E; Pettersson U
Clin Genet; 1986 Oct; 30(4):249-54. PubMed ID: 2878749
[TBL] [Abstract][Full Text] [Related]
15. Implications of fragile X expression in normal males for the nature of the mutation.
Ledbetter DH; Ledbetter SA; Nussbaum RL
Nature; 1986 Nov 13-19; 324(6093):161-3. PubMed ID: 3785381
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Molecular markers of fragile X: clinical aspects of carrier detection and prenatal diagnosis.
Murphy PD; Wilmot PL; Shapiro LR
Prog Clin Biol Res; 1991; 368():59-72. PubMed ID: 1682943
[TBL] [Abstract][Full Text] [Related]
18. Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere.
Mulligan LM; Grover HJ; Blanchette VS; Giles AR; Lillicrap DP; Phillips A; Holden JJ; White BN
Am J Med Genet; 1987 Mar; 26(3):751-60. PubMed ID: 3105317
[TBL] [Abstract][Full Text] [Related]
19. Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.
Vincent A; Heitz D; Petit C; Kretz C; Oberlé I; Mandel JL
Nature; 1991 Feb; 349(6310):624-6. PubMed ID: 1672039
[TBL] [Abstract][Full Text] [Related]
20. X-linked mental retardation: a study of 7 families.
Jacobs PA; Glover TW; Mayer M; Fox P; Gerrard JW; Dunn HG; Herbst DS
Am J Med Genet; 1980; 7(4):471-89. PubMed ID: 7211957
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
