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5. Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM). Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH. Hum Genet; 1989 Mar; 81(4):308-10. PubMed ID: 2703233 [Abstract] [Full Text] [Related]
6. 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; 46(6):1073-81. PubMed ID: 1971149 [Abstract] [Full Text] [Related]
16. 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 [Abstract] [Full Text] [Related]
17. Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locus. Smeets HJ, Hermens R, Brunner HG, Ropers HH, Wieringa B. Genomics; 1991 Feb; 9(2):257-63. PubMed ID: 1840564 [Abstract] [Full Text] [Related]
18. Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis. Lavedan C, Duros C, Savoy D, Leblond S, Bailly J, Korneluk R, Junien C. Genomics; 1990 Dec; 8(4):739-40. PubMed ID: 1980487 [No Abstract] [Full Text] [Related]
19. Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19. Mohrenweiser HW, Carrano AV, Fertitta A, Perry B, Thompson LH, Tucker JD, Weber CA. Cytogenet Cell Genet; 1989 Dec; 52(1-2):11-4. PubMed ID: 2558854 [Abstract] [Full Text] [Related]