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.
7. Genetic mapping of a second myotonic dystrophy locus. Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781 [TBL] [Abstract][Full Text] [Related]
8. Human genetics. The costs of instability. Davies KE Nature; 1992 Mar; 356(6364):15. PubMed ID: 1538769 [No Abstract] [Full Text] [Related]
9. Mutable mutation. Some genes cause diseases by growing and growing and.. Rennie J Sci Am; 1992 May; 266(5):34. PubMed ID: 1566039 [No Abstract] [Full Text] [Related]
10. 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. Trinucleotide repeat instability: when and where? Nelson DL; Warren ST Nat Genet; 1993 Jun; 4(2):107-8. PubMed ID: 8348143 [No Abstract] [Full Text] [Related]
12. Inheritance and pathogenicity of myotonic dystrophy. Johnson K Mol Cell Biol Hum Dis Ser; 1993; 3():85-110. PubMed ID: 8111546 [No Abstract] [Full Text] [Related]
13. Direct detection of novel expanded trinucleotide repeats in the human genome. Schalling M; Hudson TJ; Buetow KH; Housman DE Nat Genet; 1993 Jun; 4(2):135-9. PubMed ID: 8348150 [TBL] [Abstract][Full Text] [Related]
14. Confirmation of a gene for multiple sclerosis (MS) to chromosome region 19q13.3. Lucotte GL; Genet Couns; 2002; 13(2):133-8. PubMed ID: 12150212 [TBL] [Abstract][Full Text] [Related]
15. [The role of trinucleotide repeats in human genetic diseases]. Hietanen K Duodecim; 1996; 112(3):188-93. PubMed ID: 10590627 [No Abstract] [Full Text] [Related]
16. [Perinatal asphyxia as incorrect explanation for mental retardation]. Tuerlings JH; Smits AP; van den Berg PP Ned Tijdschr Geneeskd; 2002 Sep; 146(38):1765-8. PubMed ID: 12369434 [TBL] [Abstract][Full Text] [Related]