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Journal Abstract Search

93 related items for PubMed ID: 7835440

  • 1. The molecular biology of Norrie's disease.
    Black G, Redmond RM.
    Eye (Lond); 1994; 8 ( Pt 5)():491-6. PubMed ID: 7835440
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  • 2. A genetic linkage study of a family with Norrie's disease.
    Esakowitz L, Clark C, Haites N, Kelly K, Johnston AW.
    Eye (Lond); 1988; 2 ( Pt 4)():443-7. PubMed ID: 3253138
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  • 3. Norrie's disease.
    Johnston SS, Hanna JE, Nevin NC, Bryars JH.
    Birth Defects Orig Artic Ser; 1982; 18(6):729-38. PubMed ID: 6890861
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  • 4. Unusual presentation of Norrie's disease with hypomagnesemia.
    Kumar MS, Shenoi A, Mukta Jain M, Ashok J, Chidananda SC, Sameera P, Maseeuddin S.
    Indian Pediatr; 1998 Aug; 35(8):783-6. PubMed ID: 10216575
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  • 12. Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.
    Phillips CI, Newton M, Duvall J, Holloway S, Levy AM.
    Br J Ophthalmol; 1986 Apr; 70(4):305-13. PubMed ID: 3964631
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  • 14. [X-linked mental retardation and X-chromosome fragile sites (author's transl)].
    Schmidt A, Passarge E.
    Dtsch Med Wochenschr; 1981 Apr 10; 106(15):460-3. PubMed ID: 7215173
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  • 20. Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysis.
    Polomeno RC, Zeesman S, MacDonald IM, Crozier DG, Tenniswood MP, Kaplan P.
    Can J Ophthalmol; 1987 Feb 10; 22(1):21-3. PubMed ID: 3815151
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