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Journal Abstract Search

148 related items for PubMed ID: 8298651

  • 1. Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1.
    Casey B, Devoto M, Jones KL, Ballabio A.
    Nat Genet; 1993 Dec; 5(4):403-7. PubMed ID: 8298651
    [Abstract] [Full Text] [Related]

  • 2. Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
    Hardcastle AJ, Thiselton DL, Zito I, Ebenezer N, Mah TS, Gorin MB, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2000 Jul; 41(8):2080-6. PubMed ID: 10892847
    [Abstract] [Full Text] [Related]

  • 3. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
    Gedeon AK, Glass IA, Connor JM, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):121-4. PubMed ID: 8826461
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  • 4. X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects.
    Mathias RS, Lacro RV, Jones KL.
    Am J Med Genet; 1987 Sep 12; 28(1):111-6. PubMed ID: 3674105
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  • 5. Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1.
    Figuera LE, Pandolfo M, Dunne PW, Cantú JM, Patel PI.
    Nat Genet; 1995 Jun 12; 10(2):202-7. PubMed ID: 7663516
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  • 6. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
    Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.
    J Clin Invest; 1993 Jun 12; 91(6):2351-7. PubMed ID: 8099916
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  • 7. 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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  • 8. Situs inversus totalis and a novel ZIC3 mutation in a family with X-linked heterotaxy.
    D'Alessandro LC, Casey B, Siu VM.
    Congenit Heart Dis; 2013 Jul 12; 8(2):E36-40. PubMed ID: 22171628
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  • 10. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug 12; 43(8):2540-5. PubMed ID: 12147582
    [Abstract] [Full Text] [Related]

  • 11. X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.
    Schwartz M, Haim M, Skarsholm D.
    Clin Genet; 1990 Oct 12; 38(4):281-6. PubMed ID: 1980096
    [Abstract] [Full Text] [Related]

  • 12. Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28).
    Hoar DI, Field LL, Beards F, Hoganson G, Rollnick B, Hoo JJ.
    Am J Med Genet; 1992 Jan 15; 42(2):170-2. PubMed ID: 1733165
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  • 13. 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
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  • 14. Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
    Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M.
    Am J Med Genet; 1993 Apr 15; 46(2):172-5. PubMed ID: 8484404
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  • 16. Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings.
    Hamel BC, Smits AP, Otten BJ, van den Helm B, Ropers HH, Mariman EC.
    Am J Med Genet; 1996 Jul 12; 64(1):35-41. PubMed ID: 8826446
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  • 19. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
    Manolis EN, Eavey RD, Sangwatanaroj S, Halpin C, Rosenbaum S, Watkins H, Jarcho J, Seidman CE, Seidman JG.
    Am J Otol; 1999 Sep 12; 20(5):621-6. PubMed ID: 10503584
    [Abstract] [Full Text] [Related]

  • 20. X-linked laterality sequence in a family with carrier manifestations.
    Mikkilä SP, Janas M, Karikoski R, Tarkkila T, Simola KO.
    Am J Med Genet; 1994 Feb 15; 49(4):435-8. PubMed ID: 8160739
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