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4. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q. Johnson K; Nimmo E; Jones P; Weiss M; Savontaus ML; Anvret M; Bartlett R; Roses A; Shaw D; Harper PS Hum Genet; 1988 Dec; 80(4):379-81. PubMed ID: 3198115 [TBL] [Abstract][Full Text] [Related]
5. Clinical and genetic heterogeneity in myotonic dystrophies. Meola G Muscle Nerve; 2000 Dec; 23(12):1789-99. PubMed ID: 11102902 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Myotonic dystrophy reviewed: back to the future? Wieringa B Hum Mol Genet; 1994 Jan; 3(1):1-7. PubMed ID: 8162011 [No Abstract] [Full Text] [Related]
8. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19. Shaw DJ; Meredith AL; Sarfarazi M; Harley HG; Huson SM; Brook JD; Bufton L; Litt M; Mohandas T; Harper PS Hum Genet; 1986 Nov; 74(3):262-6. PubMed ID: 2877933 [TBL] [Abstract][Full Text] [Related]
9. Definition of subchromosomal intervals around the myotonic dystrophy locus at 19q. Brunner H; Coerwinkel-Driessen M; Smeets B; Schonk D; Schepens J; Oerlemans F; Hamel B; Ropers H; Wieringa B Prog Clin Biol Res; 1989; 306():107-14. PubMed ID: 2740406 [No Abstract] [Full Text] [Related]
11. 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]
12. Genetic and physical demarcation of the locus for dystrophia myotonica. Wieringa B; Brunner H; Hulsebos T; Schonk D; Ropers HH Adv Neurol; 1988; 48():47-69. PubMed ID: 2891258 [No Abstract] [Full Text] [Related]
13. Proximal weakness as the primary manifestation of myotonic dystrophy in older adults. Lacomis D; Chad DA; Smith TW Muscle Nerve; 1994 Jun; 17(6):687-8. PubMed ID: 8196716 [No Abstract] [Full Text] [Related]
14. The use of apolipoprotein CII as a genetic marker for myotonic dystrophy. Bird TD; Boehnke M; Schellenberg GD; Deeb SS; Lipe HP Arch Neurol; 1987 Mar; 44(3):273-5. PubMed ID: 2881531 [TBL] [Abstract][Full Text] [Related]
15. Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Aslanidis C; Jansen G; Amemiya C; Shutler G; Mahadevan M; Tsilfidis C; Chen C; Alleman J; Wormskamp NG; Vooijs M Nature; 1992 Feb; 355(6360):548-51. PubMed ID: 1346925 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q. Jansen G; de Jong PJ; Amemiya C; Aslanidis C; Shaw DJ; Harley HG; Brook JD; Fenwick R; Korneluk RG; Tsilfidis C Genomics; 1992 Jul; 13(3):509-17. PubMed ID: 1639379 [TBL] [Abstract][Full Text] [Related]
20. Multiple familial pilomatricomas: a cutaneous marker for myotonic dystrophy. Delfino M; Monfrecola G; Ayala F; Suppa F; Piccirillo A Dermatologica; 1985; 170(3):128-32. PubMed ID: 3979639 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]