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Journal Abstract Search

144 related items for PubMed ID: 9545411

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  • 2. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G.
    Mol Vis; 2005 Nov 03; 11():934-40. PubMed ID: 16288197
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  • 3. Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly.
    Jordan T, Ebenezer N, Manners R, McGill J, Bhattacharya S.
    Am J Hum Genet; 1997 Oct 03; 61(4):882-8. PubMed ID: 9382099
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  • 5. 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 03; 116(1):154-162.e1. PubMed ID: 19004499
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  • 6. Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.
    Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM.
    J Med Genet; 2003 Jan 03; 40(1):37-41. PubMed ID: 12525540
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  • 9. A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.
    Mackay D, Ionides A, Berry V, Moore A, Bhattacharya S, Shiels A.
    Am J Hum Genet; 1997 Jun 03; 60(6):1474-8. PubMed ID: 9199569
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  • 13. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
    Pang CP, Fan BJ, Canlas O, Wang DY, Dubois S, Tam PO, Lam DS, Raymond V, Ritch R.
    Mol Vis; 2006 Feb 14; 12():85-92. PubMed ID: 16518310
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  • 15. Congenital microcoria in a Saudi family.
    Al-Owaid A, Alarfaj M, Al-Qahtani A, Al-Arfaj K.
    Ophthalmic Genet; 2019 Dec 14; 40(6):578-580. PubMed ID: 31755798
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  • 20. Probable exclusion of GLC1A as a candidate glaucoma gene in a family with middle-age-onset primary open-angle glaucoma.
    Richards JE, Lichter PR, Herman S, Hauser ER, Hou YC, Johnson AT, Boehnke M.
    Ophthalmology; 1996 Jul 14; 103(7):1035-40. PubMed ID: 8684791
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