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8. A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. Tyynismaa H; Sistonen P; Tuupanen S; Tervo T; Dammert A; Latvala T; Alitalo T Invest Ophthalmol Vis Sci; 2002 Oct; 43(10):3160-4. PubMed ID: 12356819 [TBL] [Abstract][Full Text] [Related]
9. [Genetics of conical cornea (author's transl)]. Hammerstein W Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1974; 190(4):293-308. PubMed ID: 4547927 [No Abstract] [Full Text] [Related]
10. [A familial case of keratoconus with corneal granular dystrophy]. Mitsui M; Sakimoto T; Sawa M; Katami M Nippon Ganka Gakkai Zasshi; 1996 Nov; 100(11):916-9. PubMed ID: 8953898 [TBL] [Abstract][Full Text] [Related]
11. [Significance of the sex ratio in the determination of x-chromosomal heredity demonstrated on the clinical picture of keratoconus]. Hammerstein W Klin Monbl Augenheilkd; 1971 Nov; 159(5):602-8. PubMed ID: 5136278 [No Abstract] [Full Text] [Related]
13. [Pseudokeratoconus in trisomy 21 and posterior polymorphous corneal dystrophy]. Lang GK; Holbach L; Schlötzer U Klin Monbl Augenheilkd; 1989 Aug; 195(2):95-9. PubMed ID: 2529395 [TBL] [Abstract][Full Text] [Related]
14. A syndrome of nerve deafness, eye anomalies and Marfanoid habitus with autosomal dominant inheritance. Walker BA Birth Defects Orig Artic Ser; 1971 Mar; 07(4):137-9. PubMed ID: 5173345 [No Abstract] [Full Text] [Related]
15. Mutations in the zinc finger protein gene, ZNF469, contribute to the pathogenesis of keratoconus. Vincent AL; Jordan CA; Cadzow MJ; Merriman TR; McGhee CN Invest Ophthalmol Vis Sci; 2014 Aug; 55(9):5629-35. PubMed ID: 25097247 [TBL] [Abstract][Full Text] [Related]
16. VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. Bisceglia L; Ciaschetti M; De Bonis P; Campo PA; Pizzicoli C; Scala C; Grifa M; Ciavarella P; Delle Noci N; Vaira F; Macaluso C; Zelante L Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):39-45. PubMed ID: 15623752 [TBL] [Abstract][Full Text] [Related]
17. Evidence for keratoconus susceptibility locus on chromosome 14: a genome-wide linkage screen using single-nucleotide polymorphism markers. Liskova P; Hysi PG; Waseem N; Ebenezer ND; Bhattacharya SS; Tuft SJ Arch Ophthalmol; 2010 Sep; 128(9):1191-5. PubMed ID: 20837804 [TBL] [Abstract][Full Text] [Related]