173 related articles for article (PubMed ID: 1968042)
21. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.
Suthers GK; Hyland VJ; Callen DF; Oberle I; Rocchi M; Thomas NS; Morris CP; Schwartz CE; Schmidt M; Ropers HH
Am J Hum Genet; 1990 Aug; 47(2):187-95. PubMed ID: 2378346
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. A new DNA marker tightly linked to the fragile X locus (FRAXA).
Suthers GK; Callen DF; Hyland VJ; Kozman HM; Baker E; Eyre H; Harper PS; Roberts SH; Hors-Cayla MC; Davies KE
Science; 1989 Dec; 246(4935):1298-300. PubMed ID: 2573953
[TBL] [Abstract][Full Text] [Related]
26. RN1, a new polymorphic marker near the fragile X locus. (HGM10 assignment DXS 369).
Hupkes PE; van Bennekom CA; van Oost BA; Oostra BA
Nucleic Acids Res; 1990 Feb; 18(3):692. PubMed ID: 1968631
[No Abstract] [Full Text] [Related]
27. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
Brown WT; Gross AC; Chan CB; Jenkins EC
Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome.
Rekilä AM; Väisänen ML; Kähkönen M; Leisti J; Winqvist R
Hum Genet; 1988 Oct; 80(2):193. PubMed ID: 2902001
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. 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]
34. Pulsed-field gradient-gel studies around the fragile site.
Dobkin CS; Brown WT
Am J Med Genet; 1988; 30(1-2):593-600. PubMed ID: 2902798
[TBL] [Abstract][Full Text] [Related]
35. Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.
Patterson MN; Bell MV; Bloomfield J; Flint T; Dorkins H; Thibodeau SN; Schaid D; Bren G; Schwartz CE; Wieringa B
Genomics; 1989 May; 4(4):570-8. PubMed ID: 2744766
[TBL] [Abstract][Full Text] [Related]
36. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL
Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701
[TBL] [Abstract][Full Text] [Related]
37. Genetic linkage heterogeneity in the fragile X syndrome.
Brown WT; Gross AC; Chan CB; Jenkins EC
Hum Genet; 1985; 71(1):11-8. PubMed ID: 2993154
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis.
Forster-Gibson CJ; Mulligan LM; Simpson NE; White BN; Holden JJ
Am J Med Genet; 1986; 23(1-2):665-83. PubMed ID: 3006491
[TBL] [Abstract][Full Text] [Related]
40. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.
Hofker MH; Bergen AA; Skraastad MI; Carpenter NJ; Veenema H; Connor JM; Bakker E; van Ommen GJ; Pearson PL
Am J Hum Genet; 1987 Apr; 40(4):312-28. PubMed ID: 2883888
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
