88 related articles for article (PubMed ID: 1708201)
1. Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site.
Siniscalco M; Oberlé I; Melis P; Alhadeff B; Murray J; Filippi G; Mattioni T; Chen YT; Furneaux H; Old LJ
Am J Med Genet; 1991; 38(2-3):357-62. PubMed ID: 1708201
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site.
Hirst MC; Bell MV; MacKinnon RN; Watson JE; Callen D; Sutherland G; Dahl N; Patterson MN; Schwartz C; Ledbetter D
Am J Med Genet; 1991; 38(2-3):354-6. PubMed ID: 1673311
[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. 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 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]
12. 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]
13. 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]
14. 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]
15. Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.
van Oost BA; Smits A; Dreesen JC; Smeets D; Perdon L; van Bennekom CA; Dahl N; Bakker E; Oostra BA
Am J Med Genet; 1991; 38(2-3):328-31. PubMed ID: 2018075
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.
Schnur RE; Ledbetter SA; Ledbetter DH; Merry DE; Nussbaum RL
Am J Hum Genet; 1989 Feb; 44(2):248-54. PubMed ID: 2563194
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA.
Sauer SM; Phelan MC; Richer CL; Schwartz CE
Cytogenet Cell Genet; 1989; 50(2-3):172-3. PubMed ID: 2776486
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]