121 related articles for article (PubMed ID: 2018075)
1. 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]
2. 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]
3. 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]
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. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.
Brown WT; Gross AC; Goonewardena P; Ferrando C; Dobkin C; Jenkins EC
Am J Med Genet; 1991; 38(2-3):343-6. PubMed ID: 1673308
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. New polymorphic DNA marker close to the fragile site FRAXA.
Oostra BA; Hupkes PE; Perdon LF; van Bennekom CA; Bakker E; Halley DJ; Schmidt M; Du Sart D; Smits A; Wieringa B
Genomics; 1990 Jan; 6(1):129-32. PubMed ID: 1968042
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. New distal marker closely linked to the fragile X locus.
Hulsebos TJ; Oostra BA; Broersen S; Smits A; van Oost BA; Westerveld A
Hum Genet; 1991 Jul; 87(3):369-72. PubMed ID: 1677926
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis and carrier detection in fragile X.
von Koskull H; Nordström AM; Salonen R; Peltonen L
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):174-80. PubMed ID: 1605189
[TBL] [Abstract][Full Text] [Related]
19. New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.
Rousseau F; Vincent A; Oberlé I; Mandel JL
Hum Genet; 1990 Feb; 84(3):263-6. PubMed ID: 1968034
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
