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29. Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19. Eiberg H; Mohr J; Nielsen LS; Simonsen N Clin Genet; 1983 Sep; 24(3):159-70. PubMed ID: 6627719 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers. Norman AM; Floyd JL; Meredith AL; Harper PS J Med Genet; 1989 Dec; 26(12):750-4. PubMed ID: 2575669 [TBL] [Abstract][Full Text] [Related]
33. Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19. Pericak-Vance MA; Yamaoka LH; Assinder RI; Hung WY; Bartlett RJ; Stajich JM; Gaskell PC; Ross DA; Sherman S; Fey GH Neurology; 1986 Nov; 36(11):1418-23. PubMed ID: 3762959 [TBL] [Abstract][Full Text] [Related]
34. Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings. Ashizawa T; Dunne CJ; Dubel JR; Perryman MB; Epstein HF; Boerwinkle E; Hejtmancik JF Neurology; 1992 Oct; 42(10):1871-7. PubMed ID: 1407565 [TBL] [Abstract][Full Text] [Related]
35. Coincidence of neurofibromatosis and myotonic dystrophy in a kindred. Ichikawa K; Crosley CJ; Culebras A; Weitkamp L J Med Genet; 1981 Apr; 18(2):134-8. PubMed ID: 6787200 [TBL] [Abstract][Full Text] [Related]
37. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai]. Xie H; Zheng H; Zheng S; Deng B; Xu J; Cui Y; Wang Y; Xu Z; Ren D Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):319-22. PubMed ID: 11024209 [TBL] [Abstract][Full Text] [Related]
38. Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms. Bailly J; MacKenzie AE; Leblond S; Korneluk RG Hum Genet; 1991 Mar; 86(5):457-62. PubMed ID: 2016086 [TBL] [Abstract][Full Text] [Related]