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Journal Abstract Search

287 related items for PubMed ID: 9849063

  • 1. [Familial heterotaxy syndrome. Case report and review of the international literature].
    Cesko I, Hajdú J, Marton T, Tarnai L, Zs Tóth E.
    Orv Hetil; 1998 Nov 15; 139(46):2775-8. PubMed ID: 9849063
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  • 2. Polysplenia and situs inversus in siblings. Case reports.
    Cesko I, Hajdú J, Marton T, Tarnai L, Papp Z.
    Fetal Diagn Ther; 2001 Nov 15; 16(1):1-3. PubMed ID: 11125242
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  • 3. Ivemark syndrome with asplenia in siblings.
    Cesko I, Hajdú J, Tóth T, Marton T, Papp C, Papp Z.
    J Pediatr; 1997 May 15; 130(5):822-4. PubMed ID: 9152295
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  • 4. [Ivemark syndrome: 2 case reports].
    Roth P, Agnani G, Arbez-Gindre F, Roux C, Martin A, Colette C.
    J Gynecol Obstet Biol Reprod (Paris); 1993 May 15; 22(7):771-5. PubMed ID: 8308205
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  • 6. Dextrocardia with and without situs viscerum inversus in two sibs.
    Distefano G, Romeo MG, Grasso S, Mazzone D, Sciacca P, Mollica F.
    Am J Med Genet; 1987 Aug 15; 27(4):929-34. PubMed ID: 3425603
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  • 8. A case report of polysplenia syndrome associated with genital tract duplication anomaly.
    Engineer N, Scheimberg I, Akinfenwa Y.
    J Perinat Med; 2004 Aug 15; 32(4):381-2. PubMed ID: 15346829
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  • 13. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL, Bixler D, Girod D.
    Am J Med Genet; 1983 Sep 15; 16(1):35-42. PubMed ID: 6638068
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  • 15. Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature.
    Noack F, Sayk F, Ressel A, Berg C, Gembruch U, Reusche E.
    Prenat Diagn; 2002 Nov 15; 22(11):1011-5. PubMed ID: 12424766
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  • 17. Technetium-99m-sulfur colloid SPECT imaging in infants with suspected heterotaxy syndrome.
    Oates E, Austin JM, Becker JL.
    J Nucl Med; 1995 Aug 15; 36(8):1368-71. PubMed ID: 7629579
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  • 18. Craniorachischisis and heterotaxia with heart disease in twins: link or change nature?
    Bianca S, Bartoloni G, Barone C, Barrano B, Boemi G, De Filippo V, Indaco L, Cataliotti A, Ettore G.
    Congenit Heart Dis; 2010 Aug 15; 5(5):450-3. PubMed ID: 21087431
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  • 19. Prenatal diagnosis of a complex fetal cardiac malformation associated with asplenia.
    Mauser I, Deutinger J, Bernaschek G.
    Br Heart J; 1991 May 15; 65(5):293-5. PubMed ID: 2039676
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