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Journal Abstract Search


192 related items for PubMed ID: 2729348

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Hypogenitalism in the acrocallosal syndrome.
    Temtamy SA, Meguid NA.
    Am J Med Genet; 1989 Mar; 32(3):301-5. PubMed ID: 2658583
    [Abstract] [Full Text] [Related]

  • 3. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A, Schmid W.
    Am J Med Genet; 1980 Mar; 6(3):241-9. PubMed ID: 7424976
    [Abstract] [Full Text] [Related]

  • 4. 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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  • 6. 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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  • 8. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA, Legat G, Trautmann U.
    Ann Genet; 1992 Dec 18; 35(1):41-6. PubMed ID: 1610119
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  • 9. [Familial agenesis of the corpus callosum: a new form].
    Castro-Gago M, Rodriguez-Nuñez A, Eiris J, Peña J, Tojo R, Novo-Rodriguez I.
    Arch Fr Pediatr; 1993 Apr 18; 50(4):327-30. PubMed ID: 8379821
    [Abstract] [Full Text] [Related]

  • 10. The acrocallosal syndrome.
    Nelson MM, Thomson AJ.
    Am J Med Genet; 1982 Jun 18; 12(2):195-9. PubMed ID: 7102724
    [Abstract] [Full Text] [Related]

  • 11. Opitz trigonocephaly syndrome.
    Haaf T, Hofmann R, Schmid M.
    Am J Med Genet; 1991 Sep 15; 40(4):444-6. PubMed ID: 1746609
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  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. [The acrocallosal syndrome. Report of an additional case].
    Wendisch J, Lorenz P, Kabus M, Rupprecht E, Walther S.
    Kinderarztl Prax; 1990 Jun 01; 58(6):315-21. PubMed ID: 2166860
    [Abstract] [Full Text] [Related]

  • 15. Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome.
    Courtens W, Vamos E, Christophe C, Schinzel A.
    Am J Med Genet; 1997 Mar 03; 69(1):17-22. PubMed ID: 9066878
    [Abstract] [Full Text] [Related]

  • 16. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS.
    Am J Med Genet; 1994 Jun 01; 51(2):98-101. PubMed ID: 8092201
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  • 17. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A, Colletto GM, Gollop TR, Masiero D.
    Am J Med Genet; 1985 Apr 01; 20(4):631-8. PubMed ID: 2986457
    [Abstract] [Full Text] [Related]

  • 18. Acrocallosal syndrome: additional manifestations.
    Casamassima AC, Beneck D, Gewitz MH, Horowitz MA, Woolf PK, Pettersen IM, Shapiro LR.
    Am J Med Genet; 1989 Mar 01; 32(3):311-7. PubMed ID: 2658584
    [Abstract] [Full Text] [Related]

  • 19. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects.
    Zlotogora J, Glick B.
    Am J Med Genet; 1993 Aug 01; 47(1):89-90. PubMed ID: 8368260
    [Abstract] [Full Text] [Related]

  • 20. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
    da-Silva EO.
    Am J Med Genet; 1988 Apr 01; 29(4):837-43. PubMed ID: 3400727
    [Abstract] [Full Text] [Related]


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