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.
42. Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19. Shaw DJ; Meredith AL; Brook JD; Sarfarzi M; Harley HG; Huson SM; Bell GI; Harper PS Hum Genet; 1986 Nov; 74(3):267-9. PubMed ID: 2877934 [TBL] [Abstract][Full Text] [Related]
43. Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. Harley HG; Brook JD; Floyd J; Rundle SA; Crow S; Walsh KV; Thibault MC; Harper PS; Shaw DJ Am J Hum Genet; 1991 Jul; 49(1):68-75. PubMed ID: 2063878 [TBL] [Abstract][Full Text] [Related]
44. Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population. Nokelainen P; Alanen-Kurki L; Winqvist R; Falck B; Somer H; Leisti J; Johnson K; Savontaus ML; Peltonen L Hum Genet; 1990 Oct; 85(5):541-5. PubMed ID: 1977684 [TBL] [Abstract][Full Text] [Related]
45. Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism. Lavedan C; Hofmann-Radvanyi H; Shelbourne P; Rabes JP; Duros C; Savoy D; Dehaupas I; Luce S; Johnson K; Junien C Am J Hum Genet; 1993 May; 52(5):875-83. PubMed ID: 8098180 [TBL] [Abstract][Full Text] [Related]
46. Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q. Friedrich U; Brunner H; Smeets D; Lambermon E; Ropers HH Hum Genet; 1987 Mar; 75(3):291-3. PubMed ID: 2881880 [TBL] [Abstract][Full Text] [Related]
47. Myotonic dystrophy type 2 and related myotonic disorders. Meola G; Moxley RT J Neurol; 2004 Oct; 251(10):1173-82. PubMed ID: 15503094 [TBL] [Abstract][Full Text] [Related]
48. [Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion]. Spranger M; Janssen B; Rating D; Spranger S Nervenarzt; 1999 Feb; 70(2):131-5. PubMed ID: 10098148 [TBL] [Abstract][Full Text] [Related]
49. Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy. Shutler G; MacKenzie AE; Brunner H; Wieringa B; de Jong P; Lohman FP; Leblond S; Bailly J; Korneluk RG Genomics; 1991 Mar; 9(3):500-4. PubMed ID: 1674498 [TBL] [Abstract][Full Text] [Related]
50. 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]
51. Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)? Abbruzzese C; Krahe R; Liguori M; Tessarolo D; Siciliano MJ; Ashizawa T; Giacanelli M J Neurol; 1996 Oct; 243(10):715-21. PubMed ID: 8923304 [TBL] [Abstract][Full Text] [Related]
52. [The RFLP of LDR152/PstI in the Chinese and its application to linkage analysis in a myotonic dystrophy family]. Tan J; Qiu XF; Xue JL; Liu ZD; Li YS; Zai CH Yi Chuan Xue Bao; 1991; 18(1):6-11. PubMed ID: 1674205 [TBL] [Abstract][Full Text] [Related]
54. Identification of new DNA markers close to the myotonic dystrophy locus. Brook JD; Harley HG; Walsh KV; Rundle SA; Siciliano MJ; Harper PS; Shaw DJ J Med Genet; 1991 Feb; 28(2):84-8. PubMed ID: 1672160 [TBL] [Abstract][Full Text] [Related]
55. "Shake hands"; diagnosing a floppy infant--myotonic dystrophy and the congenital subtype: a difficult perinatal diagnosis. Verrijn Stuart AA; Huisman M; van Straaten HL; Bakker JC; Arabin B J Perinat Med; 2000; 28(6):497-501. PubMed ID: 11155437 [TBL] [Abstract][Full Text] [Related]
56. Recombination events that locate myotonic dystrophy distal to APOC2 on 19q. Johnson K; Shelbourne P; Davies J; Buxton J; Nimmo E; Anvret M; Bonduelle M; Williamson B; Savontaus ML Genomics; 1989 Nov; 5(4):746-51. PubMed ID: 2591962 [TBL] [Abstract][Full Text] [Related]