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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
143 related items for PubMed ID: 1670748
21. 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 [Abstract] [Full Text] [Related]
22. 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 Nov; 38(2-3):298-304. PubMed ID: 1673301 [Abstract] [Full Text] [Related]
23. DXS539, a polymorphic DNA marker proximal of the fragile-X gene. Dreesen JC, van den Hurk JA, Smits AP, van den Ouweland AM, Markslag PW, van Oost BA. Hum Genet; 1993 Mar; 91(1):80-2. PubMed ID: 8454292 [Abstract] [Full Text] [Related]
24. 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 [Abstract] [Full Text] [Related]
25. 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 Sep; 38(2-3):319-21. PubMed ID: 1673304 [Abstract] [Full Text] [Related]
26. 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 01; 43(6):1050-6. PubMed ID: 1415337 [Abstract] [Full Text] [Related]
27. 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 Aug 01; 38(2-3):357-62. PubMed ID: 1708201 [Abstract] [Full Text] [Related]
28. Prenatal diagnosis and carrier detection in fragile X. von Koskull H, Nordström AM, Salonen R, Peltonen L. Am J Med Genet; 1991 Aug 01; 43(1-2):174-80. PubMed ID: 1605189 [Abstract] [Full Text] [Related]
29. A new DNA probe of potential use for diagnosis of the fragile-X syndrome. Lucotte G. Ann Genet; 1990 Aug 01; 33(2):109-10. PubMed ID: 1978629 [Abstract] [Full Text] [Related]
32. Improved DNA markers for efficient analysis of fragile X families. Heilig R, Oberlé I, Arveiler B, Hanauer A, Vidaud M, Mandel JL. Am J Med Genet; 1988 Aug 01; 30(1-2):543-50. PubMed ID: 2902795 [Abstract] [Full Text] [Related]
33. Rapid preparation of diagnostic probes for the fragile X syndrome by direct PCR amplification of human chromosomal DNA. Yamauchi M, Seki N, Hori T. Jpn J Hum Genet; 1992 Sep 01; 37(3):195-203. PubMed ID: 1472701 [Abstract] [Full Text] [Related]
34. 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 01; 24(1):14-22. PubMed ID: 2879932 [Abstract] [Full Text] [Related]
35. 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 Jan 01; 38(2-3):354-6. PubMed ID: 1673311 [Abstract] [Full Text] [Related]
36. A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus. Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S. Am J Hum Genet; 1990 Jun 01; 46(6):1073-81. PubMed ID: 1971149 [Abstract] [Full Text] [Related]
37. Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome. Dahl N, Hammarström-Heeroma K, Goonewardena P, Wadelius C, Gustavson KH, Holmgren G, van Ommen GJ, Pettersson U. Hum Genet; 1989 Jun 01; 82(3):216-8. PubMed ID: 2567272 [Abstract] [Full Text] [Related]
38. Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island. Heitz D, Rousseau F, Devys D, Saccone S, Abderrahim H, Le Paslier D, Cohen D, Vincent A, Toniolo D, Della Valle G. Science; 1991 Mar 08; 251(4998):1236-9. PubMed ID: 2006411 [Abstract] [Full Text] [Related]
39. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus. Sood R, Mulligan LM, Poon R, White BN, Holden JJ. Am J Hum Genet; 1990 Sep 08; 47(3):395-402. PubMed ID: 1975476 [Abstract] [Full Text] [Related]
40. Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site. Richards RI, Holman K, Kozman H, Kremer E, Lynch M, Pritchard M, Yu S, Mulley J, Sutherland GR. J Med Genet; 1991 Dec 08; 28(12):818-23. PubMed ID: 1757956 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]