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PUBMED FOR HANDHELDS

Journal Abstract Search


149 related items for PubMed ID: 5450273

  • 21.
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  • 22. [Diagnosis of fetal diseases by examination of the amniotic fluid (author's transl)].
    Sidiropoulos D.
    Schweiz Rundsch Med Prax; 1975 Dec 09; 64(49):1567-73. PubMed ID: 54915
    [No Abstract] [Full Text] [Related]

  • 23. Lesch-Nyhan mutation: prenatal detection with amniotic fluid cells.
    DeMars R, Sarto G, Felix JS, Benke P.
    Science; 1969 Jun 13; 164(3885):1303-5. PubMed ID: 4890364
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  • 24. Diagnosis and prenatal diagnosis of lysosomal storage diseases.
    Shi HP, Guo YF, Zhang WM, Yuan LF, Luo HY, Sun NH, Zhao SM, Zhu MG.
    Chin Med J (Engl); 1988 Jun 13; 101(6):383-7. PubMed ID: 3146466
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  • 29. Observations on the coexistence of methylmalonic acidemia and glycinemia.
    Morrow G, Barness LA, Auerbach VH, DiGeorge AM, Ando T, Nyhan WL.
    J Pediatr; 1969 May 13; 74(5):680-90. PubMed ID: 5778824
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  • 30.
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  • 31. [Importance and current possibilities of prenatal diagnosis of genetically conditioned pathologic states].
    Srsen S.
    Cesk Pediatr; 1971 May 13; 26(5):240-2. PubMed ID: 5559528
    [No Abstract] [Full Text] [Related]

  • 32. Prenatal detection of genetic defects.
    Nadler HL.
    J Pediatr; 1969 Jan 13; 74(1):132-43. PubMed ID: 4882540
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  • 38. Safety and accuracy of midtrimester amniocentesis for prenatal diagnosis of genetic disorders.
    Aula P, Karjalainen O, Teramo K, Vaara L, Seppälä M.
    Ann Clin Res; 1979 Aug 13; 11(4):156-63. PubMed ID: 92907
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  • 39. [Study of the amniotic fluid and its current importance in obstetrics].
    Landes P.
    Sem Hop; 1974 May 14; 50(23):1577-80. PubMed ID: 4369678
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  • 40. [Prenatal diagnosis in hereditary metabolic diseases].
    Teller WM.
    Dtsch Med Wochenschr; 1975 Aug 15; 100(33):1674-7. PubMed ID: 1098883
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