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209 related items for PubMed ID: 2570019
21. Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library. Stolz FM, Pfau HP, Reipen G, Schnittger S, Grzeschik KH, Hansmann I. Genomics; 1991 Dec; 11(4):948-55. PubMed ID: 1686021 [Abstract] [Full Text] [Related]
22. Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA). Thomas NS, Chelly J, Zonana J, Davies KJ, Morgan S, Gault J, Rack KA, Buckle VJ, Brockdorff N, Clarke A. Hum Mol Genet; 1993 Oct; 2(10):1679-85. PubMed ID: 8268921 [Abstract] [Full Text] [Related]
23. Assignment of 35 single-copy and 17 repetitive sequence DNA probes to human chromosome 3: high-resolution physical mapping of 7 DNA probes by in situ hybridization. Atchison L, Cannizzaro L, Caamano J, Atchison M, Comis RL. Genomics; 1990 Mar; 6(3):441-50. PubMed ID: 2328989 [Abstract] [Full Text] [Related]
25. Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16. Germino GG, Barton NJ, Lamb J, Higgs DR, Harris P, Xiao GH, Scherer G, Nakamura Y, Reeders ST. Am J Hum Genet; 1990 May; 46(5):925-33. PubMed ID: 2339691 [Abstract] [Full Text] [Related]
32. Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome. Van Camp G, Stinissen P, Van Hul W, Backhovens H, Wehnert A, Vandenberge A, Van Broeckhoven C. Hum Genet; 1989 Aug; 83(1):58-60. PubMed ID: 2570018 [Abstract] [Full Text] [Related]
34. The anonymous PAS45 probe detects RFLPs in 13q31. Gross MS, Sefiani A, de Tand MF, Lau YF, Saidi-Mehtar N, Hors-Cayla MC, Frezal J, Van Cong N. Ann Genet; 1989 Aug; 32(2):73-7. PubMed ID: 2569289 [Abstract] [Full Text] [Related]