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10. Chromosomal localization of the human gene for annexin V (placental anticoagulant protein I) to 4q26----q28. Tait JF, Frankenberry DA, Shiang R, Murray JC, Adler DA, Disteche CM. Cytogenet Cell Genet; 1991 Oct 05; 57(4):187-92. PubMed ID: 1683830 [Abstract] [Full Text] [Related]
11. Genetic studies in Alzheimer's disease with an NACP/alpha-synuclein polymorphism. Xia Y, Rohan de Silva HA, Rosi BL, Yamaoka LH, Rimmler JB, Pericak-Vance MA, Roses AD, Chen X, Masliah E, DeTeresa R, Iwai A, Sundsmo M, Thomas RG, Hofstetter CR, Gregory E, Hansen LA, Katzman R, Thal LJ, Saitoh T. Ann Neurol; 1996 Aug 05; 40(2):207-15. PubMed ID: 8773602 [Abstract] [Full Text] [Related]
13. A TaqI polymorphism in the human cyclin A gene. Paterlini P, De Mitri MS, Martin C, Münnich A, Bréchot C. Nucleic Acids Res; 1991 May 11; 19(9):2516. PubMed ID: 1675006 [No Abstract] [Full Text] [Related]
14. A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPs. Surratt CK, Persico AM, Yang XD, Edgar SR, Bird GS, Hawkins AL, Griffin CA, Li X, Jabs EW, Uhl GR. FEBS Lett; 1993 Mar 08; 318(3):325-30. PubMed ID: 8095030 [Abstract] [Full Text] [Related]
15. An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4]. Verga V, Dos Santos M, Marques I, Povey S, Ramsay M, Jenkins T. Nucleic Acids Res; 1989 May 25; 17(10):4010. PubMed ID: 2567510 [No Abstract] [Full Text] [Related]
16. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL. Science; 1997 Jun 27; 276(5321):2045-7. PubMed ID: 9197268 [Abstract] [Full Text] [Related]
18. The gene for 17 beta-hydroxysteroid dehydrogenase maps to human chromosome 17, bands q12-q21, and shows an RFLP with ScaI. Winqvist R, Peltoketo H, Isomaa V, Grzeschik KH, Mannermaa A, Vihko R. Hum Genet; 1990 Oct 27; 85(5):473-6. PubMed ID: 1977681 [Abstract] [Full Text] [Related]