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Journal Abstract Search

196 related items for PubMed ID: 6360648

  • 21. Evaluation of syndromes: II. The isolated case.
    Thurmon TF.
    J La State Med Soc; 1979 Jun; 131(6):159-63. PubMed ID: 490021
    [No Abstract] [Full Text] [Related]

  • 22. [Congenital diseases, especially chromosome abnormalities and hereditary metabolism disorders].
    Brandt NJ, Philip J.
    Ugeskr Laeger; 1977 Mar 28; 139(13):774-7. PubMed ID: 847816
    [No Abstract] [Full Text] [Related]

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  • 25. [Growth disturbances in children and therapeutic possibilities].
    Trygstad O.
    Tidsskr Nor Laegeforen; 1973 Mar 20; 93(8):520-3. PubMed ID: 4697593
    [No Abstract] [Full Text] [Related]

  • 26. [Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression].
    Stoll C, Roth MP, Hessemann H, Paira M.
    Arch Fr Pediatr; 1983 Dec 20; 40(10):763-6. PubMed ID: 6673680
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  • 29. [Some reflections on the problem of encephalopathies in childhood (ideas, framework, classification)].
    Blumenfeld S.
    Ann Med Psychol (Paris); 1967 Dec 20; 2(5):715-24. PubMed ID: 5585702
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  • 31. Therapeutic modalities for genetic diseases: an overview.
    Rosenberg LE.
    Prog Clin Biol Res; 1979 Dec 20; 34():41-52. PubMed ID: 531065
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  • 34. [Genetics in medicine].
    Zerbin-Rüdin E.
    Wien Med Wochenschr; 1969 Nov 08; 119(45):759-64. PubMed ID: 5385931
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  • 37. [Genetics and pathology].
    Dubinin NP.
    Arkh Patol; 1974 Nov 08; 36(7):3-8. PubMed ID: 4451496
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  • 40. Cataracts as a manifestation of chromosomal aberration syndromes, inborn errors of metabolism, and malformation syndromes.
    Monteleone JA, Monteleone PL.
    Pediatr Ann; 1977 Jan 08; 6(1):115-22. PubMed ID: 834478
    [No Abstract] [Full Text] [Related]

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