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3. [Role of hereditary factors in the development of senile cataract]. Eremenko NS Oftalmol Zh; 1985; (7):399-402. PubMed ID: 4088563 [No Abstract] [Full Text] [Related]
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6. [Molecular genetics of hereditary cataract-hyperferritinemia syndrome]. Milon B; Beaumont C Ann Biol Clin (Paris); 1998 Jul; 56 Spec No():36-40. PubMed ID: 9827213 [No Abstract] [Full Text] [Related]
7. Ocular manifestations in a family with probably X-linked cataracts. Pavone L; La Rosa M; Sorge G; Scaletta S; Li Volti S; Mollica F Clin Genet; 1981 Oct; 20(4):243-6. PubMed ID: 6800675 [No Abstract] [Full Text] [Related]
8. A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance. Burdon KP; Wirth MG; Mackey DA; Russell-Eggitt IM; Craig JE; Elder JE; Dickinson JL; Sale MM J Med Genet; 2004 Aug; 41(8):e106. PubMed ID: 15286166 [No Abstract] [Full Text] [Related]
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12. Is there an X-linked form of congenital cataracts? Crews SJ; Bundey SE Clin Genet; 1982 May; 21(5):351-3. PubMed ID: 7116682 [No Abstract] [Full Text] [Related]
13. A progressive early onset cataract gene maps to human chromosome 17q24. Armitage MM; Kivlin JD; Ferrell RE Nat Genet; 1995 Jan; 9(1):37-40. PubMed ID: 7704021 [TBL] [Abstract][Full Text] [Related]
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17. [The Wiedemann-Beckwith syndrome and a congenital cataract]. Momtchilova M; Pelosse B; Laroche L; Vazquez MP J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983 [TBL] [Abstract][Full Text] [Related]
18. Refinement of the X-linked cataract locus (CXN) and gene analysis for CXN and Nance-Horan syndrome (NHS). Brooks S; Ebenezer N; Poopalasundaram S; Maher E; Francis P; Moore A; Hardcastle A Ophthalmic Genet; 2004 Jun; 25(2):121-31. PubMed ID: 15370543 [TBL] [Abstract][Full Text] [Related]
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