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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

62 related items for PubMed ID: 6798980

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  • 4. The pattern of thalassemia in Naples.
    Pepe G, Lupi L, Mastrobuono A, Carestia C, Lania A, Luzzatto L.
    Birth Defects Orig Artic Ser; 1982; 18(7):177-84. PubMed ID: 7159727
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  • 5. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
    Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C.
    Eur J Hum Genet; 2002 Mar; 10(3):210-2. PubMed ID: 11973626
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  • 6. Linkage disequilibrium at the cystathionine beta synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine. The Ears II Group. European Atherosclerosis Research Study.
    De Stefano V, Dekou V, Nicaud V, Chasse JF, London J, Stansbie D, Humphries SE, Gudnason V.
    Ann Hum Genet; 1998 Nov; 62(Pt 6):481-90. PubMed ID: 10363126
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  • 8. Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy).
    Asaka T, Ikeuchi K, Okino S, Takizawa Y, Satake R, Nitta E, Komai K, Endo K, Higuchi S, Oyake T, Yoshimura T, Suenaga A, Uyama E, Saito T, Konagaya M, Sunohara N, Namba R, Takada H, Honke K, Nishina M, Tanaka H, Shinagawa M, Tanaka K, Matsushima A, Tsuji S, Takamori M.
    J Hum Genet; 2001 Nov; 46(11):649-55. PubMed ID: 11721884
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  • 11. Quantifying the amount of missing information in genetic association studies.
    Nicolae DL.
    Genet Epidemiol; 2006 Dec; 30(8):703-17. PubMed ID: 16986163
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  • 14. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
    Lemsaddek W, Picanço I, Seuanes F, Mahmal L, Benchekroun S, Khattab M, Nogueira P, Osório-Almeida L.
    Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
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  • 15. Susceptibility of biallelic haplotype and genotype frequencies to genotyping error.
    Moskvina V, Schmidt KM.
    Biometrics; 2006 Dec; 62(4):1116-23. PubMed ID: 17156286
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  • 17. An allelic association study of two polymorphic markers in close proximity to a balanced translocation t(1:11) that co-segregates with mental illness.
    Wilson-Annan JC, Blackwood DH, Muir W, Millar JK, Porteous DJ.
    Psychiatr Genet; 1997 Dec; 7(4):171-4. PubMed ID: 9460802
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  • 18. Association and linkage studies between bipolar affective disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3.
    Meira-Lima IV, Zhao J, Sham P, Pereira AC, Krieger JE, Vallada H.
    Mol Psychiatry; 2001 Sep; 6(5):565-9. PubMed ID: 11526470
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  • 20. Localization of the hemochromatosis disease gene: linkage disequilibrium analysis using an American patient collection.
    Seese NK, Venditti CP, Chorney KA, Gerhard GS, Ma J, Hudson TJ, Phatak PD, Chorney MJ.
    Blood Cells Mol Dis; 1996 Sep; 22(1):36-46; discussion 47-8. PubMed ID: 8807084
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