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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

111 related items for PubMed ID: 4670473

  • 21.
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  • 22. Clinical consequences of heterozygosity for autosomal-recessive diseases.
    Vogel F.
    Clin Genet; 1984 May; 25(5):381-415. PubMed ID: 6373070
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  • 23.
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  • 25. [Familial idiopathic thrombocytopenic purpura (author's transl)].
    Msefer-Alaoui F, Bouaouda H, Lahrichi H, Benchemsi N, Baroudi A.
    Ann Pediatr (Paris); 1981 Mar; 28(3):215-20. PubMed ID: 7194619
    [No Abstract] [Full Text] [Related]

  • 26. Autosomal recessive generalized myotonia.
    Zellweger H, Pavone L, Biondi A, Cimino V, Gullotta F, Hart M, Ionasescu V, Mollica F, Schieken R.
    Muscle Nerve; 1980 Mar; 3(2):176-80. PubMed ID: 7366606
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  • 30. Genetic studies of congenital cataract.
    Mostafa MS, Temtamy S, El-Gammal MY, Sayed SI, Abdel-Salam M, El-Baroudy R.
    Metab Pediatr Ophthalmol; 1981 Mar; 5(3-4):233-42. PubMed ID: 7311663
    [No Abstract] [Full Text] [Related]

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  • 36. [Association of chronic tubulo-interstitial nephropathy and of tapeto-retinal degeneration. Genetic study].
    Bois E, Royer P.
    Arch Fr Pediatr; 1970 May; 27(5):471-81. PubMed ID: 5425823
    [No Abstract] [Full Text] [Related]

  • 37.
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  • 38. [Cardiological studies on patients with autosomal dominant and autosomal recessive hereditary myotonia congenital and myotonia dystrophica].
    Bodem R, Boikhan MS, Kuhn E.
    Verh Dtsch Ges Inn Med; 1971 May; 77():1289-90. PubMed ID: 5156008
    [No Abstract] [Full Text] [Related]

  • 39. [Genic diseases and chromosome diseases].
    Robert JM, Cordier MP.
    Soins; 1983 Apr; (403):3-6. PubMed ID: 6553367
    [No Abstract] [Full Text] [Related]

  • 40. Renal glycosuria (a family study).
    Dash R, Mishra K, Das PC, Das RK, Mohakur AC, Padhi PK, Mishra D.
    J Indian Med Assoc; 1984 Aug; 82(8):287-9. PubMed ID: 6491338
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