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Journal Abstract Search

67 related items for PubMed ID: 1583306

  • 1.
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  • 2. [Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)].
    Le Marec B, Defawe G, Mention JE, Picard F, Duval JM, Dubois J.
    J Gynecol Obstet Biol Reprod (Paris); 1980; 9(6):655-7. PubMed ID: 7462570
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  • 4. Late prenatal diagnosis of fetal trisomy 18 associated with severe intrauterine growth retardation.
    Johnson TR, Corson VL, Payne PA, Stetten G.
    Johns Hopkins Med J; 1982 Nov; 151(5):242-5. PubMed ID: 7143876
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  • 7. Trisomy 13 karyotype within 24 hours from a cord blood specimen.
    McCormack BJ, Dewan K, Shlossman PA, Brosch F, Manley JS, Tildon-Burton JE, Borgaonkar DS.
    Del Med J; 1995 Jan; 67(1):23. PubMed ID: 7867854
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  • 8. Prenatal diagnosis of complete trisomy 9: a case report and review of the literature.
    Kor-Anantakul O, Suwanrath C, Kanngurn S, Rujirabanjerd S, Suntharasaj T, Pinjaroen S.
    Am J Perinatol; 2006 Feb; 23(2):131-5. PubMed ID: 16506121
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  • 9. [Intrauterine growth retardation associated with a mosaic trisomy 20 limited to the placenta. A case report].
    Lacoste-Jugnet N, Depret-Mosser S, Vinatier D, Savary D, Dufour P, Lefebvre-Maunoury C, Monnier JC.
    J Gynecol Obstet Biol Reprod (Paris); 1995 Feb; 24(6):606-9. PubMed ID: 8830080
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  • 10. Complex mosaicism associated with trisomy 9.
    Smoleniec JS, Davies T, Lunt P, Berry PJ, James D.
    Prenat Diagn; 1993 Mar; 13(3):211-3. PubMed ID: 8506220
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  • 11. Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.
    Chitayat D, Hodgkinson K, Luke A, Winsor E, Rose T, Kalousek D.
    Am J Med Genet; 1995 Apr 10; 56(3):247-51. PubMed ID: 7778583
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  • 12. A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
    Roberts E, Dunlop J, Davis GS, Churchill D, Davison EV.
    Prenat Diagn; 2003 Jul 10; 23(7):564-5. PubMed ID: 12868084
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  • 14. Prenatal diagnosis of mosaicism for triploidy and trisomy 13.
    Phelan MC, Curtis Rogers R, Michaelis RC, Moore CL, Blackburn W.
    Prenat Diagn; 2001 Jun 10; 21(6):457-60. PubMed ID: 11438949
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  • 15. [Pätau syndrome without trisomy karyotype? Danger of restricted thinking in syndrome diagnosis].
    Rode G, Duda V.
    Z Geburtshilfe Perinatol; 1991 Jun 10; 195(3):143-5. PubMed ID: 1926974
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  • 16. Fryns syndrome phenotype and trisomy 22.
    Ladonne JM, Gaillard D, Carré-Pigeon F, Gabriel R.
    Am J Med Genet; 1996 Jan 02; 61(1):68-70. PubMed ID: 8741922
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  • 17. Prenatal diagnosis of a partial 6q trisomy: a case report.
    Valerio D, Di Domenico A, Felicetti M, La Boccetta A, Ferrara C, Antonio N, Borrelli AL.
    Prenat Diagn; 2006 Oct 02; 26(10):917-9. PubMed ID: 16845680
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  • 19. A normative study of obstetric complications associated with fetal trisomy 18.
    Saller DN, Oyer CE, Star J, Canick JA.
    J Perinatol; 1996 Oct 02; 16(2 Pt 1):117-20; quiz 121-2. PubMed ID: 8732559
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  • 20. Prenatal diagnosis of trisomy 3 mosaicism.
    Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J.
    Prenat Diagn; 2004 Sep 02; 24(9):693-6. PubMed ID: 15386452
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