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Journal Abstract Search

221 related items for PubMed ID: 10398231

  • 21. Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.
    Moore GE, Williamson R, Jensson O, Chambers J, Takakubo F, Newton R, Balacs MA, Ivens A.
    J Craniofac Genet Dev Biol; 1991; 11(4):372-6. PubMed ID: 1687471
    [Abstract] [Full Text] [Related]

  • 22. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
    Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, McIntosh I.
    Eur J Hum Genet; 2003 Nov; 11(11):835-9. PubMed ID: 14571267
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region.
    Robledo R, Melis P, Laficara F, Marchi J, Rinaldi A, Siniscalco M, Filippi G.
    Am J Med Genet; 1996 Jul 12; 64(1):107-12. PubMed ID: 8826459
    [Abstract] [Full Text] [Related]

  • 26. A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.
    Uyguner O, Kayserili H, Li Y, Karaman B, Nürnberg G, Hennies H, Becker C, Nürnberg P, Başaran S, Apak MY, Wollnik B.
    Clin Genet; 2007 Mar 12; 71(3):212-9. PubMed ID: 17309643
    [Abstract] [Full Text] [Related]

  • 27. 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 Mar 12; 36(4):194-9. PubMed ID: 8166423
    [Abstract] [Full Text] [Related]

  • 28. Linkage localization of Börjeson-Forssman-Lehmann syndrome.
    Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA.
    Am J Med Genet; 1989 Dec 12; 34(4):470-4. PubMed ID: 2624254
    [Abstract] [Full Text] [Related]

  • 29. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN).
    Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC.
    Ophthalmic Genet; 2000 Dec 12; 21(4):227-33. PubMed ID: 11135493
    [Abstract] [Full Text] [Related]

  • 30. TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment.
    Gomot M, Ronce N, Dessay S, Zemni R, Ayrault AD, Moizard MP, Nivelon A, Gilgenkrantz S, Dourlens J, Des Portes V, Chelly J, Moraine C.
    Am J Med Genet; 2002 Nov 01; 112(4):400-4. PubMed ID: 12376945
    [Abstract] [Full Text] [Related]

  • 31. X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.
    Raynaud M, Gendrot C, Dessay B, Moncla A, Ayrault AD, Moizard MP, Toutain A, Briault S, Villard L, Ronce N, Moraine C.
    Am J Med Genet; 1996 Jul 12; 64(1):97-106. PubMed ID: 8826458
    [Abstract] [Full Text] [Related]

  • 32. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D, Hadley DW, Tifft CJ, Biesecker LG.
    Am J Med Genet; 2002 Jul 15; 110(4):308-14. PubMed ID: 12116202
    [Abstract] [Full Text] [Related]

  • 33. Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31.
    Shrimpton AE, Daly KM, Hoo JJ.
    Am J Med Genet; 1999 May 28; 84(3):293-9. PubMed ID: 10331611
    [Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11.
    Strømme P, Sundet K, Mørk C, Cassiman JJ, Fryns JP, Claes S.
    J Med Genet; 1999 May 15; 36(5):374-8. PubMed ID: 10353782
    [Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38. X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.
    Galjaard RJ, Kostakoglu N, Hoogeboom JJ, Breedveld GJ, van der Linde HC, Hovius SE, Oostra BA, Sandkuijl LA, Akarsu AN, Heutink P.
    Eur J Hum Genet; 2001 Sep 15; 9(9):653-8. PubMed ID: 11571552
    [Abstract] [Full Text] [Related]

  • 39. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
    Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J.
    Eur J Hum Genet; 2001 Oct 15; 9(10):747-52. PubMed ID: 11781685
    [Abstract] [Full Text] [Related]

  • 40. 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
    [Abstract] [Full Text] [Related]

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