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Journal Abstract Search

80 related items for PubMed ID: 2882725

  • 1. How to find a mutation behind an inherited disease.
    Peltonen L, Pulkkinen L.
    Ann Clin Res; 1986; 18(5-6):224-30. PubMed ID: 2882725
    [Abstract] [Full Text] [Related]

  • 2. Looking for epilepsy genes: clinical and molecular genetic studies.
    Delgado-Escueta AV, White R, Greenberg DA, Treiman LJ.
    Adv Neurol; 1986; 44():77-95. PubMed ID: 3010682
    [Abstract] [Full Text] [Related]

  • 3. [Diagnosis using PCR: the indirect approach].
    Pillet N, Schorderet DF.
    Schweiz Rundsch Med Prax; 1994 May 17; 83(20):599-603. PubMed ID: 8209129
    [Abstract] [Full Text] [Related]

  • 4. A highly polymorphic locus very tightly linked to the Huntington's disease gene.
    Wasmuth JJ, Hewitt J, Smith B, Allard D, Haines JL, Skarecky D, Partlow E, Hayden MR.
    Nature; 1988 Apr 21; 332(6166):734-6. PubMed ID: 2895895
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  • 5. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK.
    Dan Med Bull; 2002 Nov 21; 49(4):318-45. PubMed ID: 12553167
    [Abstract] [Full Text] [Related]

  • 6. New DNA-analysis techniques (minireview).
    Coutelle C.
    Biomed Biochim Acta; 1991 Nov 21; 50(1):3-10. PubMed ID: 1677562
    [Abstract] [Full Text] [Related]

  • 7. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 21; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

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  • 9. Detection of hotspot mutations and polymorphisms using an enhanced PCR-RFLP approach.
    Liu WH, Kaur M, Makrigiorgos GM.
    Hum Mutat; 2003 May 21; 21(5):535-41. PubMed ID: 12673796
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  • 13. Search for the familial Alzheimer's disease gene.
    St George-Hyslop P, Polinsky R, Haines J, Nee L, Tanzi R, Conneally P, Growdon J, Myers R, Pollen D, Drachman D.
    J Neural Transm Suppl; 1987 May 21; 24():13-21. PubMed ID: 2890708
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  • 15. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.
    Dean M.
    Hum Mutat; 2003 Oct 21; 22(4):261-74. PubMed ID: 12955713
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  • 17. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL, Ji L, Li YD.
    Yi Chuan Xue Bao; 2004 May 21; 31(5):431-43. PubMed ID: 15478601
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  • 19. Systematic gene mapping in man: data management considerations.
    Pericak-Vance MA, Hung WY, Yamaoka L, Haynes C, Bartlett RJ, Vance JM, Lee J, Siddique T, Gaskell PC, Stajich J.
    Aust Paediatr J; 1988 May 21; 24 Suppl 1():87-9. PubMed ID: 2904804
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