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Journal Abstract Search

230 related items for PubMed ID: 3400727

  • 1. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
    da-Silva EO.
    Am J Med Genet; 1988 Apr; 29(4):837-43. PubMed ID: 3400727
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  • 2. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
    Verloes A, Dodinval P, Beco L, Bonnivert J, Lambotte C.
    Am J Med Genet; 1990 Sep; 37(1):119-23. PubMed ID: 2240028
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  • 3. Delineation of the da-Silva syndrome.
    Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K.
    Am J Med Genet; 1994 Feb 01; 49(3):313-6. PubMed ID: 8209892
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  • 4. A syndrome of microcephaly, eye anomalies, short stature, and mental deficiency.
    Bouwes Bavinck JN, Weaver DD, Ellis FD, Ward RE.
    Am J Med Genet; 1987 Apr 01; 26(4):825-31. PubMed ID: 3109242
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  • 6. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
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  • 12. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May 01; 36(1):89-93. PubMed ID: 2333912
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  • 13. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul 01; 141(7):584-6. PubMed ID: 8413337
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  • 14. X-linked mental retardation and neurological symptoms: a nosological approach.
    Schrander-Stumpel CT, Höweler CJ, Fryns JP.
    Genet Couns; 1995 Jul 01; 6(1):21-32. PubMed ID: 7794558
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  • 16. Agenesis of corpus callosum in three sibs.
    Naritomi K, Chinen Y, Asato Y.
    Jpn J Hum Genet; 1997 Dec 01; 42(4):539-41. PubMed ID: 9560954
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  • 17. Apparently new MCA/MR syndrome in sibs with cleft lip and palate and other facial, eye, heart, and intestinal anomalies.
    Kapur S, Toriello HV.
    Am J Med Genet; 1991 Dec 15; 41(4):423-5. PubMed ID: 1776630
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