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Journal Abstract Search

147 related items for PubMed ID: 34582953

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  • 3. Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features.
    Le H, Jin E, Jewell A, Jackson-Cook C, Haskell GT, Couser N.
    Am J Med Genet A; 2023 Jun; 191(6):1639-1645. PubMed ID: 36941760
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  • 6. Influence of the vitreolenticular interface in pediatric cataract surgery.
    Van Looveren J, Vael A, Ideler N, Sillen H, Mathysen D, Tassignon MJ.
    J Cataract Refract Surg; 2018 Oct; 44(10):1203-1210. PubMed ID: 30172568
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  • 8. 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; 116(1):154-162.e1. PubMed ID: 19004499
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  • 9. Septo-optic dysplasia associated with bilateral complex microphthalmos.
    Gündüz K, Günalp I, Saatçi I.
    Ophthalmic Genet; 1996 Sep; 17(3):109-13. PubMed ID: 8905851
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  • 11. Microphthalmia and anterior segment dysgenesis due to a double gene variant in GJA8 and CRYGC.
    Zhou L, Wang G, Hu B, Jiang H, Jiang F, Xu Z.
    Eur J Ophthalmol; 2024 Jan; 34(1):NP12-NP17. PubMed ID: 36916241
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  • 12. Persistent fetal vasculature and minimal fetal vascular remnants: a frequent cause of unilateral congenital cataracts.
    Müllner-Eidenböck A, Amon M, Moser E, Klebermass N.
    Ophthalmology; 2004 May; 111(5):906-13. PubMed ID: 15121367
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  • 15. Temporal iridofundal coloboma with persistent pupillary membranes with persistent fetal vasculature.
    Gupta S, Sethi HS, Naik M.
    Indian J Ophthalmol; 2020 Aug; 68(8):1649-1650. PubMed ID: 32709803
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  • 16. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
    Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, Halimi P, Roche O, Van Regemorter N, Munier F, Schorderet D, Dufier JL, Marsac C, Ricquier D, Menasche M, Penfornis A, Abitbol M.
    Mol Vis; 2007 Apr 02; 13():511-23. PubMed ID: 17417613
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  • 19. Anterior segment developmental anomalies in a 33-week-old fetus with MIDAS syndrome.
    Herwig MC, Loeffler KU, Gembruch U, Kuchelmeister K, Müller AM.
    Pediatr Dev Pathol; 2014 Apr 02; 17(6):491-5. PubMed ID: 25291437
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  • 20. Five cases of microphthalmia with other ocular malformations.
    Lee JS, Lee JE, Shin YG, Choi HY, Oum BS, Kim HJ.
    Korean J Ophthalmol; 2001 Jun 02; 15(1):41-7. PubMed ID: 11534546
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