128 related articles for article (PubMed ID: 1351365)
1. Linkage and risk assessment in fragile X families using new DNA probes at Xq27.
Carpenter NJ; Swartz-Boyd J; Prichard JK; Lam T
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):312-9. PubMed ID: 1351365
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Linkage homogeneity near the fragile X locus in normal and fragile X families.
Suthers GK; Mulley JC; Voelckel MA; Dahl N; Väisänen ML; Steinbach P; Glass IA; Schwartz CE; van Oost BA; Thibodeau SN
Genomics; 1991 Jul; 10(3):576-82. PubMed ID: 1889808
[TBL] [Abstract][Full Text] [Related]
4. Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.
Oostra BA; Majoor-Krakauer DF; van Hemel JO; Bakker E; Callen DF; Schmidt M; van Oost BA
Am J Med Genet; 1991; 38(2-3):332-5. PubMed ID: 1673306
[TBL] [Abstract][Full Text] [Related]
5. Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.
Suthers GK; Mulley JC; Voelckel MA; Dahl N; Väisänen ML; Steinbach P; Glass IA; Schwartz CE; van Oost BA; Thibodeau SN
Am J Hum Genet; 1991 Mar; 48(3):460-7. PubMed ID: 1671806
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA).
Rousseau F; Vincent A; Rivella S; Heitz D; Triboli C; Maestrini E; Warren ST; Suthers GK; Goodfellow P; Mandel JL
Am J Hum Genet; 1991 Jan; 48(1):108-16. PubMed ID: 1670748
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304.
Dahl N; Malmgren H; Pettersson U; Holmgren G; Seemanová E; Gustavson KH
Am J Med Genet; 1991; 38(2-3):319-21. PubMed ID: 1673304
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience.
Glass IA; Del Mastro RG; Lanyon WG; Raeburn JA; Kilpatrick MW; Webb TP; Connor JM
Am J Med Genet; 1992 Aug; 43(6):1050-6. PubMed ID: 1415337
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval.
Oberlé I; Vincent A; Abbadi N; Rousseau F; Hupkes PE; Hors-Cayla MC; Gilgenkrantz S; Oostra BA; Mandel JL
Am J Med Genet; 1991; 38(2-3):336-42. PubMed ID: 1673307
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
