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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

114 related items for PubMed ID: 3772853

  • 21.
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  • 22. [Hereditary brachydactyly with nail aplasia].
    Santos HG, George FH, Ferreira JR.
    Acta Med Port; 1981; 3(2):147-60. PubMed ID: 7315521
    [No Abstract] [Full Text] [Related]

  • 23.
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  • 24. [A case of hereditary hypodontia of all the molars in the upper jaw].
    Spetalen E.
    Nor Tannlaegeforen Tid; 1971 Feb; 81(2):118-21. PubMed ID: 5279905
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  • 27. Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
    Futatani T, Nii E, Obata M, Ichida F, Okabe Y, Kanegane H, Miyawaki T.
    Pediatr Int; 2008 Feb; 50(1):116-8. PubMed ID: 18279219
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  • 30. Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging.
    Bohlega S, Stigsby B, al-Kawi MZ, McLean DR, Ozand P, Omer S, Coates P.
    Mov Disord; 1995 Jul; 10(4):513-7. PubMed ID: 7565837
    [Abstract] [Full Text] [Related]

  • 31. [Pedigree analysis of two families with Alport's syndrome].
    Wässer S, Theile H, Schöne D, Lemme B.
    Padiatr Grenzgeb; 1980 Jul; 19(3):167-71. PubMed ID: 7454376
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  • 32.
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  • 34. Mode of inheritance in systemic lupus erythematosus in Saudi multiplex families.
    Qari A, Al-Mayouf S, Al-Owain M.
    Genet Couns; 2009 Jul; 20(3):215-23. PubMed ID: 19852427
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. [Nonne-Milroy-Meige disease in 2 members of a family].
    Jeske J, Ostrowska-Stach H, Hübner H.
    Pol Tyg Lek; 1969 Sep 09; 24(36):1389-90. PubMed ID: 5351081
    [No Abstract] [Full Text] [Related]

  • 37. Are 1q plus chromosomes harmless?
    Gardner RJ, McCreanor HR, Parslow MI, Veale AM.
    Clin Genet; 1974 Sep 09; 6(5):383-93. PubMed ID: 4434654
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  • 38.
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