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Journal Abstract Search

307 related items for PubMed ID: 19526372

  • 1. A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.
    Hmani-Aifa M, Ben Salem S, Benzina Z, Bouassida W, Messaoud R, Turki K, Khairallah M, Rebaï A, Fakhfekh F, Söderkvist P, Ayadi H.
    Hum Genet; 2009 Oct; 126(4):575-87. PubMed ID: 19526372
    [Abstract] [Full Text] [Related]

  • 2. Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene.
    Said MB, Chouchène E, Salem SB, Daoud K, Largueche L, Bouassida W, Benzina Z, Ayadi H, Söderkvist P, Matri L, Hmani-Aifa M.
    Gene; 2013 Oct 10; 528(2):288-94. PubMed ID: 23820083
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  • 3. A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.
    Abouzeid H, Meire FM, Osman I, ElShakankiri N, Bolay S, Munier FL, Schorderet DF.
    Ophthalmology; 2009 Jan 10; 116(1):154-162.e1. PubMed ID: 19004499
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  • 4. [Preliminary linkage analysis on autosomal dominant microphthalmia with 12 microsatellite markers].
    Yu P, Zhou Q, Guo L, Zhou YM, Luo YY, Zhang RY, Yan XY, Ding KP, Hong ZF, Zhang YZ.
    Shi Yan Sheng Wu Xue Bao; 2004 Apr 10; 37(2):85-90. PubMed ID: 15259979
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  • 5. Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families.
    Ammar M, Bouchlaka-Souissi C, Helms CA, Zaraa I, Jordan CT, Anbunathan H, Bouhaha R, Kouidhi S, Doss N, Dhaoui R, Ben Osman A, Ben Ammar El Gaied A, Marrakchi R, Mokni M, Bowcock AM.
    Br J Dermatol; 2013 Mar 10; 168(3):583-7. PubMed ID: 23013406
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  • 6. A novel locus for congenital simple microphthalmia family mapping to 17p12-q12.
    Hu Z, Yu C, Li J, Wang Y, Liu D, Xiang X, Su W, Pan Q, Xie L, Xia K.
    Invest Ophthalmol Vis Sci; 2011 May 18; 52(6):3425-9. PubMed ID: 21345985
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  • 12. Mutations in a novel serine protease PRSS56 in families with nanophthalmos.
    Orr A, Dubé MP, Zenteno JC, Jiang H, Asselin G, Evans SC, Caqueret A, Lakosha H, Letourneau L, Marcadier J, Matsuoka M, Macgillivray C, Nightingale M, Papillon-Cavanagh S, Perry S, Provost S, Ludman M, Guernsey DL, Samuels ME.
    Mol Vis; 2011 May 18; 17():1850-61. PubMed ID: 21850159
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  • 14. Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18.
    Tetens J, Ganter M, Müller G, Drögemüller C.
    Invest Ophthalmol Vis Sci; 2007 Aug 18; 48(8):3506-15. PubMed ID: 17652717
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  • 16. Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.
    Iseri SU, Wyatt AW, Nürnberg G, Kluck C, Nürnberg P, Holder GE, Blair E, Salt A, Ragge NK.
    Hum Genet; 2010 Jul 18; 128(1):51-60. PubMed ID: 20414678
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  • 17. Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan.
    Rafiq MA, Ansar M, Marshall CR, Noor A, Shaheen N, Mowjoodi A, Khan MA, Ali G, Amin-ud-Din M, Feuk L, Vincent JB, Scherer SW.
    Clin Genet; 2010 Nov 18; 78(5):478-83. PubMed ID: 20345473
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  • 18. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
    Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C.
    Nat Genet; 1994 Jul 18; 7(3):425-8. PubMed ID: 7920663
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