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Journal Abstract Search

249 related items for PubMed ID: 8456840

  • 1. New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death.
    Gustavson KH, Annerén G, Malmgren H, Dahl N, Ljunggren CG, Bäckman H.
    Am J Med Genet; 1993 Mar 01; 45(5):654-8. PubMed ID: 8456840
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  • 2. A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region.
    Hamel BC, Wesseling P, Renier WO, van den Helm B, Ropers HH, Kremer H, Mariman EC.
    J Med Genet; 1999 Feb 01; 36(2):140-3. PubMed ID: 10051014
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  • 3. MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder.
    Leshinsky-Silver E, Zinger A, Bibi CN, Barash V, Sadeh M, Lev D, Sagie TL.
    Eur J Hum Genet; 2002 Apr 01; 10(4):226-30. PubMed ID: 12032729
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  • 4. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome.
    Seemanová E, Lesný I.
    Am J Med Genet; 1996 Dec 11; 66(2):179-83. PubMed ID: 8958326
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  • 6. 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 11; 17(1):323-32. PubMed ID: 6538752
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  • 9. The FG syndrome: further characterization, report of a third family, and of a sporadic case.
    Riccardi VM, Hässler E, Lubinsky MS.
    Am J Med Genet; 1977 Jan 11; 1(1):47-58. PubMed ID: 565138
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  • 10. The Borjeson-Forssman-Lehmann syndrome. A family study.
    Dereymaeker AM, Fryns JP, Hoefnagels M, Heremans G, Marien J, van den Berghe H.
    Clin Genet; 1986 Apr 11; 29(4):317-20. PubMed ID: 3720009
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  • 11. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
    Wittwer B, Kircheisen R, Leutelt J, Orth U, Gal A.
    Am J Med Genet; 1996 Jul 12; 64(1):42-9. PubMed ID: 8826447
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  • 12. A form of X-linked mental retardation with marfanoid habitus.
    Lujan JE, Carlin ME, Lubs HA.
    Am J Med Genet; 1984 Jan 12; 17(1):311-22. PubMed ID: 6711603
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  • 13. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.
    Chudley AE, Lowry RB, Hoar DI.
    Am J Med Genet; 1988 Dec 12; 31(4):741-51. PubMed ID: 3239563
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  • 15. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
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  • 16. The X-linked syndrome of macroorchidism and mental retardation: further observations.
    Bowen P, Biederman B, Swallow KA.
    Am J Med Genet; 1978 Jul 15; 2(4):409-14. PubMed ID: 263449
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  • 17. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A.
    Genet Couns; 1999 Jul 15; 10(3):265-9. PubMed ID: 10546098
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  • 18. A new X-linked mental retardation-overgrowth syndrome.
    Golabi M, Rosen L.
    Am J Med Genet; 1984 Jan 15; 17(1):345-58. PubMed ID: 6538755
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  • 19. Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
    Shrimpton AE, Braddock BR, Hoo JJ.
    Am J Med Genet; 2000 May 15; 92(2):155-6. PubMed ID: 10797443
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  • 20. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French family.
    Lefort G, Taib J, Toutain A, Houdayer C, Moraine CI, Humeau C, Sarda P.
    Ann Genet; 1993 May 15; 36(4):200-5. PubMed ID: 8166424
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