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PUBMED FOR HANDHELDS

Journal Abstract Search


254 related items for PubMed ID: 9679615

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  • 4. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: a new kindred with severe genital anomalies and mild hematologic expression.
    McPherson EW, Clemens MM, Gibbons RJ, Higgs DR.
    Am J Med Genet; 1995 Jan 30; 55(3):302-6. PubMed ID: 7726227
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  • 6. Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome.
    Doerfler W, Wieczorek D, Gillessen-Kaesbach G, Albrecht B, Passarge E.
    Am J Med Genet; 1997 Dec 12; 73(2):210-6. PubMed ID: 9409875
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  • 11. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
    Reardon W, Gibbons RJ, Winter RM, Baraitser M.
    Am J Med Genet; 1995 Jan 30; 55(3):285-7. PubMed ID: 7726224
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  • 12. Smith-Fineman-Myers syndrome: report of a third case.
    Stephenson LD, Johnson JP.
    Am J Med Genet; 1985 Oct 30; 22(2):301-4. PubMed ID: 4050861
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  • 14. Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?
    Saugier-Veber P, Munnich A, Lyonnet S, Toutain A, Moraine C, Piussan C, Mathieu M, Gibbons RJ.
    Am J Med Genet; 1995 Jan 30; 55(3):300-1. PubMed ID: 7726226
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  • 15. 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 30; 26(4):825-31. PubMed ID: 3109242
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  • 16. A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness.
    Schimke RN, Horton WA, Collins DL, Therou L.
    Am J Med Genet; 1984 Jan 30; 17(1):323-32. PubMed ID: 6538752
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  • 17. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS, Wisniewski K, Brown WT.
    Am J Med Genet; 1994 Jul 15; 51(4):586-90. PubMed ID: 7943044
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  • 20. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
    Taysi K, Sekhon GS, Hillman RE.
    Am J Med Genet; 1982 Dec 15; 13(4):423-30. PubMed ID: 7158642
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