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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

231 related items for PubMed ID: 9409875

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  • 6. 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; 36(1):89-93. PubMed ID: 2333912
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  • 9. Filippi syndrome: report of three additional cases.
    Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.
    Am J Med Genet; 1999 Nov 19; 87(2):128-33. PubMed ID: 10533026
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  • 10. GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome.
    Verloes A, Delfortrie J, Lambotte C.
    Am J Med Genet; 1989 Jan 19; 32(1):15-8. PubMed ID: 2705477
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  • 11. Changing phenotype in Floating-Harbor syndrome.
    Hersh JH, Groom KR, Yen FF, Verdi GD.
    Am J Med Genet; 1998 Feb 26; 76(1):58-61. PubMed ID: 9508066
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  • 14. Mental retardation, microcephaly and blepharochalasis in brothers.
    Reardon W, Winter RM, Wilson J, Baraitser M.
    Clin Dysmorphol; 1994 Apr 26; 3(2):128-31. PubMed ID: 8055132
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  • 15. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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  • 18. Drayer's syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2-->qter).
    Rump P, Dijkhuizen T, Sikkema-Raddatz B, Lemmink HH, Vos YJ, Verheij JB, van Ravenswaaij CM.
    Clin Genet; 2008 Nov 01; 74(5):455-62. PubMed ID: 18651844
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  • 19. 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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  • 20. 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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