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Journal Abstract Search
87 related items for PubMed ID: 7836855
21. Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families. Watts GD, O'Briant KC, Chance PF. Hum Genet; 2002 Feb; 110(2):166-72. PubMed ID: 11935323 [Abstract] [Full Text] [Related]
22. Heterologous mitochondrial DNA recombination in human cells. D'Aurelio M, Gajewski CD, Lin MT, Mauck WM, Shao LZ, Lenaz G, Moraes CT, Manfredi G. Hum Mol Genet; 2004 Dec 15; 13(24):3171-9. PubMed ID: 15496432 [Abstract] [Full Text] [Related]
24. Vitamin D receptor: no evidence for allele-specific mRNA stability in cells which are heterozygous for the Taq I restriction enzyme polymorphism. Verbeek W, Gombart AF, Shiohara M, Campbell M, Koeffler HP. Biochem Biophys Res Commun; 1997 Sep 08; 238(1):77-80. PubMed ID: 9299455 [Abstract] [Full Text] [Related]
25. PCR detection of the Taq1 restriction fragment length polymorphism linked to the ataxia telangiectasia locus. Athma P, Liu J, Swift M. Clin Chem; 1995 Apr 08; 41(4):625-6. PubMed ID: 7720261 [No Abstract] [Full Text] [Related]
26. A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23. Hernandez D, McConville CM, Stacey M, Woods CG, Brown MM, Shutt P, Rysiecki G, Taylor AM. J Med Genet; 1993 Feb 08; 30(2):135-40. PubMed ID: 8445618 [Abstract] [Full Text] [Related]
28. Ataxia-telangiectasia in Italy: genetic analysis. Chessa L, Lisa A, Fiorani O, Zei G. Int J Radiat Biol; 1994 Dec 08; 66(6 Suppl):S31-3. PubMed ID: 7836850 [Abstract] [Full Text] [Related]
31. Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool. Berliner N, Duby AD, Morton CC, Leder P, Seidman JG. J Clin Invest; 1985 Sep 08; 76(3):1283-5. PubMed ID: 2995449 [Abstract] [Full Text] [Related]
36. [DNA polymorphism and genetic diseases]. Baiget M. Med Clin (Barc); 1986 May 10; 86(18):774-7. PubMed ID: 3526011 [No Abstract] [Full Text] [Related]
37. A TaqI site identifies the *A allele at the ACP1 locus. Sensabaugh GF, Lazaruk KA. Hum Mol Genet; 1993 Jul 10; 2(7):1079. PubMed ID: 8364553 [No Abstract] [Full Text] [Related]
38. Detection of novel genetic markers by mismatch analysis. Roberts RG, Montandon AJ, Bobrow M, Bentley DR. Nucleic Acids Res; 1989 Aug 11; 17(15):5961-71. PubMed ID: 2570401 [Abstract] [Full Text] [Related]
39. Considerations affecting the feasibility of mapping a single-gene disorder using restriction fragment polymorphisms, with special reference to ataxia-telangiectasia. Botstein D. Kroc Found Ser; 1985 Aug 11; 19():125-31. PubMed ID: 3864934 [No Abstract] [Full Text] [Related]