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Journal Abstract Search

208 related items for PubMed ID: 10797443

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: redefining a clinical entity.
    Horn D, Krebsová A, Kunze J, Reis A.
    Am J Med Genet; 2000 Jun 05; 92(4):285-92. PubMed ID: 10842298
    [Abstract] [Full Text] [Related]

  • 5. Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.
    Hamel BC, Smits AP, van den Helm B, Smeets DF, Knoers NV, van Roosmalen T, Thoonen GH, Assman-Hulsmans CF, Ropers HH, Mariman EC, Kremer H.
    Am J Med Genet; 1999 Jul 30; 85(3):290-304. PubMed ID: 10398246
    [Abstract] [Full Text] [Related]

  • 6. Refined gene localization for the Miles-Carpenter syndrome (MCS).
    Tackels D, Schwartz CE, Carpenter NJ, Miles JH.
    Am J Med Genet; 1999 Jul 30; 85(3):221-2. PubMed ID: 10398232
    [No Abstract] [Full Text] [Related]

  • 7. Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1.
    Claes S, Volcke P, Devriendt K, Holvoet M, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1999 Jul 30; 85(3):283-7. PubMed ID: 10398244
    [Abstract] [Full Text] [Related]

  • 8. X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.
    Abidi F, Hall BD, Cadle RG, Feldman GL, Lubs HA, Ouzts LV, Arena JF, Stevenson RE, Schwartz CE.
    Am J Med Genet; 1999 Jul 30; 85(3):223-9. PubMed ID: 10398233
    [Abstract] [Full Text] [Related]

  • 9. 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 30; 9(9):653-8. PubMed ID: 11571552
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.
    Lungarotti MS, Martello C, Barboni G, Mezzetti D, Mariotti G, Calabro A.
    Am J Med Genet; 1994 Jul 15; 51(4):598-601. PubMed ID: 7943046
    [Abstract] [Full Text] [Related]

  • 12. Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.
    Forrester S, Kovach MJ, Reynolds NM, Urban R, Kimonis V.
    Am J Med Genet; 2001 Jan 01; 98(1):92-100. PubMed ID: 11426460
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 34(4):470-4. PubMed ID: 2624254
    [Abstract] [Full Text] [Related]

  • 14. Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
    Tahvanainen E, Norio R, Karila E, Ranta S, Weissenbach J, Sistonen P, de la Chapelle A.
    Nat Genet; 1994 Jun 01; 7(2):201-4. PubMed ID: 7920642
    [Abstract] [Full Text] [Related]

  • 15. A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28.
    Hamel BC, Kremer H, Wesby-van Swaay E, van den Helm B, Smits AP, Oostra BA, Ropers HH, Mariman EC.
    Am J Med Genet; 1996 Jul 12; 64(1):131-3. PubMed ID: 8826463
    [Abstract] [Full Text] [Related]

  • 16. A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25-q26.
    Cilliers DD, Parveen R, Clayton P, Cairns SA, Clarke S, Shalet SM, Black GC, Newman WG, Clayton-Smith J.
    Eur J Med Genet; 2007 Jul 12; 50(3):216-23. PubMed ID: 17369115
    [Abstract] [Full Text] [Related]

  • 17. X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family.
    Van Esch H, Zanni G, Holvoet M, Borghgraef M, Chelly J, Fryns JP, Devriendt K.
    Eur J Med Genet; 2005 Jul 12; 48(2):145-52. PubMed ID: 16053905
    [Abstract] [Full Text] [Related]

  • 18. Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3.
    Kleefstra T, Yntema HG, Oudakker AR, de Vries BB, van Bokhoven H, Hamel BC, Poppelaars FA, Ausems MG.
    Am J Med Genet; 2002 Jul 15; 110(4):410-1. PubMed ID: 12116222
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one family.
    Raynaud M, Ronce N, Ayrault AD, Francannet C, Malpuech G, Moraine C.
    Am J Med Genet; 1998 Mar 19; 76(3):255-61. PubMed ID: 9508246
    [Abstract] [Full Text] [Related]

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