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PUBMED FOR HANDHELDS

Journal Abstract Search

140 related items for PubMed ID: 52836

  • 21.
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  • 24. [The antenatal diagnosis of Bonnevie-Ullrich's syndrome. The role of ultrasound (author's transl)].
    Henrion R, Aubry MC, Aubry JP, Emmanuelli CN, Dumez Y, Oury JF.
    J Gynecol Obstet Biol Reprod (Paris); 1981; 10(8):831-7. PubMed ID: 6175679
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  • 25. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE, Appadorai V, Breg WR, Howard RO.
    Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
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  • 27. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG, McConnachie P, Hadro TA.
    Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706
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  • 29. Prenatal diagnosis of Meckel syndrome: alpha-feto protein and beta-trace protein in amniotic fluid.
    Chemke J, Miskin A, Rav-Acha Z, Porath A, Sagiv M, Katz Z.
    Clin Genet; 1977 Apr; 11(4):285-9. PubMed ID: 66999
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  • 31. Prenatal diagnosis using amniocentesis: the Christchurch experience.
    Legge M, Stewart CR, Willocks DL.
    N Z Med J; 1979 Aug 08; 90(641):95-7. PubMed ID: 91147
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  • 36. [Meckel-Gruber syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Jan 08; 14(1):32-5. PubMed ID: 8451225
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  • 38. Prenatal diagnosis of the Meckel syndrome.
    Karjalainen O, Aula P, Seppälä M, Hartikainen-Sorri AL, Ryynänen M.
    Obstet Gynecol; 1981 Jun 08; 57(6 Suppl):13S-5S. PubMed ID: 6165942
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