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25. Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites. Shaw DJ; Harley HG; Brook JD; McKeithan TW Hum Genet; 1989 Aug; 83(1):71-4. PubMed ID: 2570021 [TBL] [Abstract][Full Text] [Related]
26. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy. Johnson KJ; Jones PJ; Spurr N; Nimmo E; Davies J; Creed H; Weiss M; Williamson R Cytogenet Cell Genet; 1988; 48(1):13-5. PubMed ID: 2460293 [TBL] [Abstract][Full Text] [Related]
27. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Harley HG; Brook JD; Rundle SA; Crow S; Reardon W; Buckler AJ; Harper PS; Housman DE; Shaw DJ Nature; 1992 Feb; 355(6360):545-6. PubMed ID: 1346923 [TBL] [Abstract][Full Text] [Related]
28. Analysis of repetitive regions in myotonic dystrophy type 1 and 2. Carson NL Curr Protoc Hum Genet; 2009 Apr; Chapter 9():Unit 9.6. PubMed ID: 19360700 [TBL] [Abstract][Full Text] [Related]
29. The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q. Saunders AM; Seldin MF Genomics; 1990 Feb; 6(2):324-32. PubMed ID: 2307474 [TBL] [Abstract][Full Text] [Related]
30. Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe. Davies KE; Jackson J; Williamson R; Harper PS; Ball S; Sarfarazi M; Meredith L; Fey G J Med Genet; 1983 Aug; 20(4):259-63. PubMed ID: 6620325 [TBL] [Abstract][Full Text] [Related]
31. Further mapping of markers around the centromere of human chromosome 19. Brook JD; Skinner M; Roberts SH; Rettig WJ; Almond JW; Shaw DJ Genomics; 1987 Dec; 1(4):320-8. PubMed ID: 3482421 [TBL] [Abstract][Full Text] [Related]
32. Myotonic dystrophy and gene mapping on human chromosome 19. Brook JD; Shaw DJ; Meredith AL Biotechnol Genet Eng Rev; 1985; 3():311-47. PubMed ID: 3004536 [No Abstract] [Full Text] [Related]
33. Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers. Lavedan C; Hofmann H; Shelbourne P; Duros C; Savoy D; Johnson K; Junien C J Med Genet; 1991 Feb; 28(2):89-91. PubMed ID: 2002492 [TBL] [Abstract][Full Text] [Related]
34. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers. Takemoto Y; Miki T; Nakura J; Nishikawa K; Kamino K; Takeda S; Kuzu K; Osame M; Nakagawa M; Higuchi I Jinrui Idengaku Zasshi; 1989 Sep; 34(3):189-94. PubMed ID: 2576756 [TBL] [Abstract][Full Text] [Related]
35. A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. Smeets H; Bachinski L; Coerwinkel M; Schepens J; Hoeijmakers J; van Duin M; Grzeschik KH; Weber CA; de Jong P; Siciliano MJ Am J Hum Genet; 1990 Mar; 46(3):492-501. PubMed ID: 2309701 [TBL] [Abstract][Full Text] [Related]
36. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Buxton J; Shelbourne P; Davies J; Jones C; Van Tongeren T; Aslanidis C; de Jong P; Jansen G; Anvret M; Riley B Nature; 1992 Feb; 355(6360):547-8. PubMed ID: 1346924 [TBL] [Abstract][Full Text] [Related]
37. [Advances in molecular genetics of myotonic dystrophy]. Yamagata H; Yamanaka N; Miki T; Ogihara T Nihon Rinsho; 1993 Sep; 51(9):2474-80. PubMed ID: 8411731 [TBL] [Abstract][Full Text] [Related]
38. [Myotonic dystrophy: DNA instability in monozygotic twins]. Redondo L; Polo MA; Rodríguez F; Ramírez P; Aguilar J; Lucas M; Molano J Rev Neurol; 1999 Apr 1-15; 28(7):711-3. PubMed ID: 10363301 [TBL] [Abstract][Full Text] [Related]
39. [Myotonic dystrophy of Steinert]. Junien C J Genet Hum; 1989 Jan; 37(1):51-4. PubMed ID: 2565953 [TBL] [Abstract][Full Text] [Related]
40. Myotonic dystrophy: update on progress to define the gene. Roses AD; Pericak-Vance MA; Bartlett RJ; Yamaoka LH; Lee JE; Koh J; Chen JC; Gilbert JR; Ross DA; Herbstreith MH Aust Paediatr J; 1988; 24 Suppl 1():66-9. PubMed ID: 3060077 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]