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Journal Abstract Search

208 related items for PubMed ID: 10797443

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  • 25. Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.
    Turner G, Gedeon A, Mulley J, Sutherland G, Rae J, Power K, Arthur I.
    Am J Med Genet; 1989 Dec; 34(4):463-9. PubMed ID: 2624253
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  • 27. 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; 17(1):323-32. PubMed ID: 6538752
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  • 28. Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33).
    Holinski-Feder E, Golla A, Rost I, Seidel H, Rittinger O, Meindl A.
    Am J Med Genet; 1996 Jul 12; 64(1):125-30. PubMed ID: 8826462
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  • 32. 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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  • 33. Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
    Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M.
    Eur J Hum Genet; 2000 Feb 15; 8(2):125-9. PubMed ID: 10757644
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  • 36. X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localization.
    Turner G, Gedeon A, Mulley J.
    Am J Med Genet; 1994 Jul 15; 51(4):575-80. PubMed ID: 7943042
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  • 37. A gene for FG syndrome maps in the Xq12-q21.31 region.
    Briault S, Hill R, Shrimpton A, Zhu D, Till M, Ronce N, Margaritte-Jeannin P, Baraitser M, Middleton-Price H, Malcolm S, Thompson E, Hoo J, Wilson G, Romano C, Guichet A, Pembrey M, Fontes M, Poustka A, Moraine C.
    Am J Med Genet; 1997 Nov 28; 73(1):87-90. PubMed ID: 9375929
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  • 38. 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 28; 26(4):825-31. PubMed ID: 3109242
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  • 40. Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22.
    Donnelly AJ, Choo KH, Kozman HM, Gedeon AK, Danks DM, Mulley JC.
    Am J Med Genet; 1994 Jul 15; 51(4):581-5. PubMed ID: 7943043
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