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2. Genome mappers have a hot time at Cold Spring Harbor. Nowak R Science; 1995 May; 268(5214):1134-5. PubMed ID: 7761827 [No Abstract] [Full Text] [Related]
4. A time to sequence. Olson MV Science; 1995 Oct; 270(5235):394-6. PubMed ID: 7569992 [No Abstract] [Full Text] [Related]
5. Human genome mapping and its medical perspectives. Siniscalco M Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 2():25-46. PubMed ID: 9561634 [No Abstract] [Full Text] [Related]
6. The human cancer genome project--one more misstep in the war on cancer. Gabor Miklos GL Nat Biotechnol; 2005 May; 23(5):535-7. PubMed ID: 15877064 [No Abstract] [Full Text] [Related]
7. The Human Genome Project: implications for nursing. Lessick M; Williams J Medsurg Nurs; 1994 Feb; 3(1):49-58. PubMed ID: 8124379 [TBL] [Abstract][Full Text] [Related]
8. High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation. Neville CE; Mahadevan MS; Barceló JM; Korneluk RG Hum Mol Genet; 1994 Jan; 3(1):45-51. PubMed ID: 7909252 [TBL] [Abstract][Full Text] [Related]
10. [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]
11. Taking stock of the Genome Project. Roberts SL Science; 1993 Oct; 262(5130):20-2. PubMed ID: 8211121 [No Abstract] [Full Text] [Related]
12. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Kremer EJ; Pritchard M; Lynch M; Yu S; Holman K; Baker E; Warren ST; Schlessinger D; Sutherland GR; Richards RI Science; 1991 Jun; 252(5013):1711-4. PubMed ID: 1675488 [TBL] [Abstract][Full Text] [Related]
13. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome. Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I Mol Cell Endocrinol; 2001 Oct; 183 Suppl 1():S77-85. PubMed ID: 11576738 [TBL] [Abstract][Full Text] [Related]
14. Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. Kramer PR; Pearson CE; Sinden RR Hum Genet; 1996 Aug; 98(2):151-7. PubMed ID: 8698331 [TBL] [Abstract][Full Text] [Related]
15. [Perspectives in medical genetics: the new genetics]. Bueno M; Pérez-González JM Rev Med Univ Navarra; 1992; 37(4):181-9. PubMed ID: 1298036 [No Abstract] [Full Text] [Related]
17. 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]
18. [Myotonic dystrophy of Steinert]. Junien C J Genet Hum; 1989 Jan; 37(1):51-4. PubMed ID: 2565953 [TBL] [Abstract][Full Text] [Related]
19. [Molecular biology in medicine. XI. The Human Genome Project]. Gamba G Rev Invest Clin; 1997; 49(5):425-9. PubMed ID: 9527702 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]