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PUBMED FOR HANDHELDS

Journal Abstract Search


94 related items for PubMed ID: 2658584

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  • 2. Hypogenitalism in the acrocallosal syndrome.
    Temtamy SA, Meguid NA.
    Am J Med Genet; 1989 Mar; 32(3):301-5. PubMed ID: 2658583
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  • 6. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
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  • 8. Acrocallosal syndrome in a girl born to consanguineous parents.
    Salgado LJ, Ali CA, Castilla EE.
    Am J Med Genet; 1989 Mar; 32(3):298-300. PubMed ID: 2729348
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  • 10. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE, Kimonis VE, Morales A.
    Am J Med Genet; 1997 Dec 12; 73(2):184-8. PubMed ID: 9409870
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  • 11. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
    Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.
    Genet Couns; 2008 Dec 12; 19(2):237-40. PubMed ID: 18618999
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  • 14. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI.
    Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483
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  • 18. Agenesis of the corpus callosum, camptodactyly and obesity.
    Verloes A, Lesenfants S.
    Clin Dysmorphol; 2000 Apr 18; 9(2):107-9. PubMed ID: 10826621
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  • 19. Acrocallosal syndrome: report of a Brazilian girl.
    Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1992 Aug 01; 43(6):938-41. PubMed ID: 1415343
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