409 related articles for article (PubMed ID: 2564838)
1. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
Voelckel MA; Philip N; Piquet C; Pellissier MC; Oberlé I; Birg F; Mattei MG; Mattei JF
Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
Veenema H; Carpenter NJ; Bakker E; Hofker MH; Ward AM; Pearson PL
J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
[TBL] [Abstract][Full Text] [Related]
4. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.
Davies KE
Am J Med Genet; 1986; 23(1-2):633-42. PubMed ID: 3513572
[TBL] [Abstract][Full Text] [Related]
5. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site.
Nguyen C; Mattei MG; Rey JA; Baeteman MA; Mattei JF; Jordan BR
Am J Med Genet; 1988; 30(1-2):601-11. PubMed ID: 2902799
[TBL] [Abstract][Full Text] [Related]
6. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
Voelckel MA; Mattei MG; N'Guyen C; Philip N; Birg F; Mattei JF
Hum Genet; 1988 Dec; 80(4):375-8. PubMed ID: 2904402
[TBL] [Abstract][Full Text] [Related]
7. Increase in the incidence of the fragile site Xq27 in prometaphases.
Barbi G; Steinbach P
Hum Genet; 1982; 61(1):82. PubMed ID: 6957373
[No Abstract] [Full Text] [Related]
8. 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]
9. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
Dahl N; Goonewardena P; Malmgren H; Gustavson KH; Holmgren G; Seemanova E; Annerén G; Flood A; Pettersson U
Am J Hum Genet; 1989 Aug; 45(2):304-9. PubMed ID: 2569270
[TBL] [Abstract][Full Text] [Related]
10. [Clinical, cytogenetic and molecular aspects of fragile X syndrome].
Veenema H
Tijdschr Kindergeneeskd; 1989 Oct; 57(5):153-8. PubMed ID: 2683200
[TBL] [Abstract][Full Text] [Related]
11. The fragile X syndrome.
Brown WT
Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
[TBL] [Abstract][Full Text] [Related]
12. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
Patterson M; Bell M; Schwartz C; Davies K
Am J Med Genet; 1988; 30(1-2):581-91. PubMed ID: 3177471
[TBL] [Abstract][Full Text] [Related]
13. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
[TBL] [Abstract][Full Text] [Related]
14. Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype.
Dennis NR; Curtis G; Macpherson JN; Jacobs PA
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):232-6. PubMed ID: 1605196
[TBL] [Abstract][Full Text] [Related]
15. No genetic linkage detected for schizophrenia to Xq27-q28.
Delisi LE; Crow TJ; Davies KE; Terwilliger JD; Ott J; Ram R; Flint T; Boccio A
Br J Psychiatry; 1991 May; 158():630-4. PubMed ID: 1677599
[TBL] [Abstract][Full Text] [Related]
16. Linkage studies in a large fragile X family.
Patterson M; Bell M; Kress W; Davies KE; Froster-Iskenius U
Am J Hum Genet; 1988 Nov; 43(5):684-8. PubMed ID: 2903666
[TBL] [Abstract][Full Text] [Related]
17. Unaffected carrier males in families with fragile X syndrome.
Howard-Peebles PN; Friedman JM
Am J Hum Genet; 1985 Sep; 37(5):956-64. PubMed ID: 3863482
[TBL] [Abstract][Full Text] [Related]
18. Fragile site Xq27.3 in a family without mental retardation.
Romain DR; Chapman CJ
Clin Genet; 1992 Jan; 41(1):33-5. PubMed ID: 1633644
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
