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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 36332842

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  • 3. ROSAH syndrome mimicking chronic uveitis.
    Fardeau C, Alafaleq M, Dhaenens CM, Dollfus H, Koné-Paut I, Grunewald O, Morel JB, Titah C, Saadoun D, Lazeran PO, Meunier I.
    Clin Genet; 2023 Apr; 103(4):453-458. PubMed ID: 36543582
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  • 10. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
    Roosing S, van den Born LI, Hoyng CB, Thiadens AA, de Baere E, Collin RW, Koenekoop RK, Leroy BP, van Moll-Ramirez N, Venselaar H, Riemslag FC, Cremers FP, Klaver CC, den Hollander AI.
    Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
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  • 11. Long-term follow-up of a patient with JAG1-associated retinopathy.
    Cheema MR, Stone LG, Sellar PW, Quinn S, Clark SC, Martin RJ, O'Brien JM, Warriner C, Browning AC.
    Doc Ophthalmol; 2021 Oct; 143(2):237-247. PubMed ID: 33877487
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  • 15. Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT.
    Toma C, Ruberto G, Marzi F, Vandelli G, Signorini S, Valente EM, Antonini M, Bertone C, Bianchi PE.
    Doc Ophthalmol; 2018 Aug; 137(1):25-36. PubMed ID: 29987673
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