These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
157 related articles for article (PubMed ID: 2882476)
21. Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome. Feil R; Palmieri G; d'Urso M; Heilig R; Oberlé I; Mandel JL Am J Hum Genet; 1990 Apr; 46(4):720-8. PubMed ID: 1969226 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. 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]
26. 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]
27. 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]
28. Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage. Warren ST; Knight SJ; Peters JF; Stayton CL; Consalez GG; Zhang FP Proc Natl Acad Sci U S A; 1990 May; 87(10):3856-60. PubMed ID: 2339126 [TBL] [Abstract][Full Text] [Related]
29. An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767). Patterson M; Gitschier J; Bloomfield J; Bell M; Dorkins H; Froster-Iskenius U; Sommer S; Sobell J; Schaid D; Thibodeau S Am J Hum Genet; 1989 May; 44(5):679-85. PubMed ID: 2565080 [TBL] [Abstract][Full Text] [Related]
30. Molecular characterization of a DNA probe, U6.2, located close to the fragile X locus. Pergolizzi R; Brown WT; Goonewardena P; Bhan R; Dobkin C; Dahl N; Pettersson U Am J Med Genet; 1991; 38(2-3):380-3. PubMed ID: 1673315 [TBL] [Abstract][Full Text] [Related]
31. Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis. Vincent A; Heitz D; Petit C; Kretz C; Oberlé I; Mandel JL Nature; 1991 Feb; 349(6310):624-6. PubMed ID: 1672039 [TBL] [Abstract][Full Text] [Related]
32. X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28. Lehesjoki AE; Sankila EM; Miao J; Somer M; Salonen R; Rapola J; de la Chapelle A J Med Genet; 1990 May; 27(5):288-91. PubMed ID: 1972196 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. Physical mapping of DXS134 close to the DXS52 locus. Bell MV; Patterson MN; Dorkins HR; Davies KE Hum Genet; 1989 Apr; 82(1):27-30. PubMed ID: 2565864 [TBL] [Abstract][Full Text] [Related]
35. Limited size of the fragile X site shown by fluorescence in situ hybridization. Verkerk AJ; Eussen BH; Van Hemel JO; Oostra BA Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):187-91. PubMed ID: 1605191 [TBL] [Abstract][Full Text] [Related]
36. Characterisation of a new rare fragile site easily confused with the fragile X. Sutherland GR; Baker E Hum Mol Genet; 1992 May; 1(2):111-3. PubMed ID: 1301146 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present. Schwartz C; Fitch N; Phelan MC; Richer CL; Stevenson R Hum Genet; 1987 May; 76(1):54-7. PubMed ID: 3471705 [TBL] [Abstract][Full Text] [Related]
39. Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'. Nguyen C; Pontarotti P; Birnbaum D; Chimini G; Rey JA; Mattei JF; Jordan BR EMBO J; 1987 Nov; 6(11):3285-9. PubMed ID: 2828023 [TBL] [Abstract][Full Text] [Related]
40. Restriction fragment length polymorphisms on the q24-q28 region of X chromosome among Japanese population. Taga T; Shirahase W; Shimada M; Kurokawa K; Ueyama H Jinrui Idengaku Zasshi; 1989 Jun; 34(2):123-8. PubMed ID: 2570171 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]