165 related articles for article (PubMed ID: 2902797)
1. 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]
2. DNA linkage analysis of 26 families with fragile X syndrome.
Carpenter NJ
Am J Med Genet; 1991; 38(2-3):311-8. PubMed ID: 1673303
[TBL] [Abstract][Full Text] [Related]
3. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.
Thibodeau SN; Dorkins HR; Faulk KR; Berry R; Smith AC; Hagerman R; King A; Davies KE
Hum Genet; 1988 Jul; 79(3):219-27. PubMed ID: 3402993
[TBL] [Abstract][Full Text] [Related]
4. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.
Carpenter NJ; Thibodeau SN; Brown WT
Am J Med Genet; 1991; 38(2-3):349-53. PubMed ID: 1673310
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers.
Glass IA; Pirrit LA; White EM; Bell MV; Davies KE; Cockburn F; Connor JM
Am J Med Genet; 1991; 38(2-3):298-304. PubMed ID: 1673301
[TBL] [Abstract][Full Text] [Related]
9. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
Arveiler B; Oberlé I; Vincent A; Hofker MH; Pearson PL; Mandel JL
Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
[TBL] [Abstract][Full Text] [Related]
10. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.
Sood R; Mulligan LM; Poon R; White BN; Holden JJ
Am J Hum Genet; 1990 Sep; 47(3):395-402. PubMed ID: 1975476
[TBL] [Abstract][Full Text] [Related]
11. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
Brown WT; Ye W; Gross AC; Chan CB; Dobkin CS; Jenkins EC
Am J Med Genet; 1988; 30(1-2):551-66. PubMed ID: 2902796
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Further evidence for genetic heterogeneity in the fragile X syndrome.
Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS
Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
[TBL] [Abstract][Full Text] [Related]
14. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
Connor JM; Pirrit LA; Yates JR; Crossley JA; Imrie SJ; Colgan JM
J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
[TBL] [Abstract][Full Text] [Related]
15. Genetic mapping of new RFLPs at Xq27-q28.
Suthers GK; Oberlé I; Nancarrow J; Mulley JC; Hyland VJ; Wilson PJ; McCure J; Morris CP; Hopwood JJ; Mandel JL
Genomics; 1991 Jan; 9(1):37-43. PubMed ID: 1672291
[TBL] [Abstract][Full Text] [Related]
16. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.
Goonewardena P; Brown WT; Gross AC; Ferrando C; Dobkin C; Romano V; Bosco P; Ceratto N; Pettersson U; Dahl N
Am J Med Genet; 1991; 38(2-3):322-7. PubMed ID: 1673305
[TBL] [Abstract][Full Text] [Related]
17. Multilocus analysis of the fragile X syndrome.
Brown WT; Gross A; Chan C; Jenkins EC; Mandel JL; Oberlé I; Arveiler B; Novelli G; Thibodeau S; Hagerman R
Hum Genet; 1988 Mar; 78(3):201-5. PubMed ID: 3162224
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis.
Väisänen ML; Kähkönen M; Leisti J
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):307-11. PubMed ID: 1351364
[TBL] [Abstract][Full Text] [Related]
20. Improved DNA markers for efficient analysis of fragile X families.
Heilig R; Oberlé I; Arveiler B; Hanauer A; Vidaud M; Mandel JL
Am J Med Genet; 1988; 30(1-2):543-50. PubMed ID: 2902795
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
