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Journal Abstract Search

217 related items for PubMed ID: 574088

  • 1.
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  • 2. Heterotaxy syndrome with mirror image anomalies in identical twins.
    Thacker D, Gruber PJ, Weinberg PM, Cohen MS.
    Congenit Heart Dis; 2009; 4(1):50-3. PubMed ID: 19207405
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  • 8. [Familial asplenia syndrome].
    Jójárt G, Fekete FP.
    Acta Paediatr Acad Sci Hung; 1978; 19(1):35-40. PubMed ID: 665222
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  • 11. ["Ivemark syndrome": severe congenital cyanogenic heart disease, complex thoraco-abdominal heterotaxia and asplenia or polysplenia].
    Neimann N, Pernot C, Gentin G, Vert P, Worms AM.
    Pediatrie; 1966; 21(5):511-32. PubMed ID: 5943512
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  • 12. [On a case of Ivemark's syndrome].
    Alfieri A, Malgarini F.
    Policlinico Prat; 1967 May 29; 74(22):734-8. PubMed ID: 5611156
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  • 13. Goldenhar complex in discordant monozygotic twins: a case report and review of the literature.
    Boles DJ, Bodurtha J, Nance WE.
    Am J Med Genet; 1987 Sep 29; 28(1):103-9. PubMed ID: 3314503
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  • 15. [Surgical treatment of complex forms of congenital heart malformations associated with situs inversus (nine cases) (author's transl)].
    Pilichowski P, Hazan E, Bex JP, Dequirot A, Lecompte Y, Mathey J.
    Sem Hop; 1987 Sep 29; 56(3-4):138-43. PubMed ID: 6244644
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  • 16. The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy.
    Jacobs JP, Anderson RH, Weinberg PM, Walters HL, Tchervenkov CI, Del Duca D, Franklin RC, Aiello VD, Béland MJ, Colan SD, Gaynor JW, Krogmann ON, Kurosawa H, Maruszewski B, Stellin G, Elliott MJ.
    Cardiol Young; 2007 Sep 29; 17 Suppl 2():1-28. PubMed ID: 18039396
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  • 17. Asplenia syndrome in conjoined twins: a case report.
    Ursell PC, Wigger HJ.
    Teratology; 1983 Jun 29; 27(3):301-4. PubMed ID: 6879453
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  • 18. Risk factors for heart disease associated with abnormal sidedness.
    Kuehl KS, Loffredo C.
    Teratology; 2002 Nov 29; 66(5):242-8. PubMed ID: 12397632
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  • 20. Monozygotic Turner syndrome twins--correlation of phenotype severity and heart defect.
    Lin AE, Garver KL.
    Am J Med Genet; 1988 Mar 29; 29(3):529-31. PubMed ID: 3376996
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