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PUBMED FOR HANDHELDS

Journal Abstract Search


150 related items for PubMed ID: 10051014

  • 1. 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; 36(2):140-3. PubMed ID: 10051014
    [Abstract] [Full Text] [Related]

  • 2. Pericentromeric genes for non-specific X-linked mental retardation (MRX).
    Gedeon A, Kerr B, Mulley J, Turner G.
    Am J Med Genet; 1994 Jul 15; 51(4):553-64. PubMed ID: 7943039
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  • 3. 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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  • 4. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.
    Am J Med Genet; 1999 Jul 30; 85(3):216-20. PubMed ID: 10398231
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  • 5. A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.
    Deqaqi SC, N'Guessan M, Forner J, Sbiti A, Beldjord C, Chelly J, Sefiani A, Des Portes V.
    Ann Genet; 1998 Jul 30; 41(1):11-6. PubMed ID: 9599645
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
    Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1997 Dec 31; 73(4):474-9. PubMed ID: 9415477
    [Abstract] [Full Text] [Related]

  • 9. New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.
    Wilson M, Mulley J, Gedeon A, Robinson H, Turner G.
    Am J Med Genet; 1991 Sep 15; 40(4):406-13. PubMed ID: 1746601
    [Abstract] [Full Text] [Related]

  • 10. X-linked alpha-thalassemia/mental retardation syndrome. Linkage analysis in a new family further supports localization in proximal Xq.
    Houdayer CI, Toutain A, Ronce N, Lefort G, Sarda P, Taib J, Briault S, Lambert JC, Moraine CI.
    Ann Genet; 1993 Sep 15; 36(4):194-9. PubMed ID: 8166423
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  • 14. Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38).
    Schutz CK, Ives EJ, Chalifoux M, MacLaren L, Farrell S, Robinson PD, White BN, Holden JJ.
    Am J Med Genet; 1996 Jul 12; 64(1):89-96. PubMed ID: 8826457
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  • 17. Linkage analysis in three families with nonspecific X-linked mental retardation.
    Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P.
    Am J Med Genet; 1996 Jul 12; 64(1):137-46. PubMed ID: 8826464
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  • 18. Regional localisation of two non-specific X-linked mental retardation genes (MRX30 and MRX31).
    Donnelly AJ, Partington MW, Ryan AK, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):113-20. PubMed ID: 8826460
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  • 19. X-linked mental retardation with dystonic movements of the hands (PRTS): revisited.
    Gedeon A, Partington M, Mulley J.
    Am J Med Genet; 1994 Jul 15; 51(4):565-8. PubMed ID: 7943040
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