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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 5614980

  • 41. [Oligophrenic syndromes in children. Genetic and acquired causes; diagnostic, preventive and therapeutic possibilities].
    Saggese G.
    Minerva Pediatr; 1973; 25(21):918-40. PubMed ID: 4731706
    [No Abstract] [Full Text] [Related]

  • 42. Hearing loss associated with hereditary diseases and syndromes.
    Sataloff RT.
    Ear Nose Throat J; 1983 Nov; 62(11):571-93. PubMed ID: 6360648
    [No Abstract] [Full Text] [Related]

  • 43.
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  • 44. What is congenital disease?
    Gardner HA.
    Otolaryngol Clin North Am; 1981 Feb; 14(1):3-13. PubMed ID: 7254845
    [No Abstract] [Full Text] [Related]

  • 45. The infant cry.
    Lind J.
    Proc R Soc Med; 1971 May; 64(5):468. PubMed ID: 5576897
    [No Abstract] [Full Text] [Related]

  • 46. Plan of management for newborn babies in whom metabolic disease is anticipated or suspected.
    Danks DM.
    Clin Perinatol; 1976 Mar; 3(1):251-9. PubMed ID: 782771
    [No Abstract] [Full Text] [Related]

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  • 48. [Congenital nephrosis].
    Norio R.
    Duodecim; 1968 Mar; 84(22):1279-90. PubMed ID: 5706130
    [No Abstract] [Full Text] [Related]

  • 49. [Various unusual congenital and metabolic myopathies].
    Walton J.
    Rev Neurol (Paris); 1970 Jul; 123(1):23-8. PubMed ID: 5516327
    [No Abstract] [Full Text] [Related]

  • 50. [Attempted classification of 102 neurologic genetic diseases].
    Eskenasy J.
    Stud Cercet Neurol; 1968 Jul; 13(4):269-82. PubMed ID: 5679041
    [No Abstract] [Full Text] [Related]

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  • 54. [Treatment of some congenital metabolic errors in the mother and in the newborn infant].
    Fois A, Mattei R.
    Pediatria (Napoli); 1975 Sep 30; 83(3):479-99. PubMed ID: 1233014
    [No Abstract] [Full Text] [Related]

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  • 59. Babies at risk.
    Br Med J; 1967 May 27; 2(5551):559-60. PubMed ID: 6023993
    [No Abstract] [Full Text] [Related]

  • 60. Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.
    Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR.
    Am J Med Genet; 1982 Jan 27; 11(1):61-75. PubMed ID: 7065004
    [Abstract] [Full Text] [Related]

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