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1. Berinstein, DM; Hiraoka, M; Trese, MT; Shastry, BS
   Coats' disease and congenital retinoschisis in a single eye: A case reportand DNA analysis
   OPHTHALMOLOGICA
   
   D.M. Berinstein et al., "Coats' disease and congenital retinoschisis in a single eye: A case reportand DNA analysis", OPHTHALMOLA, 215(2), 2001, pp. 132-135
2. Curat, CA; Eck, M; Dervillez, X; Vogel, WF
   Mapping of epitopes in discoidin domain receptor 1 critical for collagen binding
   JOURNAL OF BIOLOGICAL CHEMISTRY
   
   C.A. Curat et al., "Mapping of epitopes in discoidin domain receptor 1 critical for collagen binding", J BIOL CHEM, 276(49), 2001, pp. 45952-45958
3. Huopaniemi, L; Tyynismaa, H; Rantala, A; Rosenberg, T; Alitalo, T
   Characterization of two unusual RS1 gene deletions segregating in Danish retinoschisis families
   HUMAN MUTATION
   
   L. Huopaniemi et al., "Characterization of two unusual RS1 gene deletions segregating in Danish retinoschisis families", HUM MUTAT, 16(4), 2000, pp. 307-314
4. Livesey, FJ; Furukawa, T; Steffen, MA; Church, GM; Cepko, CL
   Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx
   CURRENT BIOLOGY
   
   F.J. Livesey et al., "Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx", CURR BIOL, 10(6), 2000, pp. 301-310
5. Shastry, BS; Hiraoka, M; Trese, MT
   Lack of association of the Norrie disease gene with retinoschisis phenotype
   JAPANESE JOURNAL OF OPHTHALMOLOGY
   
   B.S. Shastry et al., "Lack of association of the Norrie disease gene with retinoschisis phenotype", JPN J OPHTH, 44(6), 2000, pp. 627-629
6. Hiriyanna, KT; Bingham, EL; Yashar, BM; Ayyagari, R; Fishman, G; Small, KW; Weinberg, DV; Weleber, RG; Lewis, RA; Andreasson, S; Richards, JE; Sieving, PA
   Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change
   HUMAN MUTATION
   
   K.T. Hiriyanna et al., "Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change", HUM MUTAT, 14(5), 1999, pp. 423-427
7. Walpole, SM; Hiriyana, KT; Nicolaou, A; Bingham, EL; Durham, J; Vaudin, M; Ross, MT; Yates, JRW; Sieving, PA; Trump, D
   Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid induced gene in Xp22
   GENOMICS
   
   S.M. Walpole et al., "Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid induced gene in Xp22", GENOMICS, 55(3), 1999, pp. 275-283
8. Kelly, J; Maumenee, IH
   Hereditary macular diseases
   INTERNATIONAL OPHTHALMOLOGY CLINICS
   
   J. Kelly e I.H. Maumenee, "Hereditary macular diseases", INT OPHTH C, 39(4), 1999, pp. 83-115
9. Gehrig, A; White, K; Lorenz, B; Andrassi, M; Clemens, S; Weber, BHF
   Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis
   CLINICAL GENETICS
   
   A. Gehrig et al., "Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis", CLIN GENET, 55(6), 1999, pp. 461-465
10. DELACHAPELLE A; WRIGHT FA
    LINKAGE DISEQUILIBRIUM MAPPING IN ISOLATED POPULATIONS - THE EXAMPLE OF FINLAND REVISITED
    Proceedings of the National Academy of Sciences of the United Statesof America
    
    A. Delachapelle e F.A. Wright, "LINKAGE DISEQUILIBRIUM MAPPING IN ISOLATED POPULATIONS - THE EXAMPLE OF FINLAND REVISITED", Proceedings of the National Academy of Sciences of the United Statesof America, 95(21), 1998, pp. 12416-12423
11. Weber, BHF
    Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula
    ACTA ANATOMICA
    
    B.H.F. Weber, "Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula", ACT ANATOM, 162(2-3), 1998, pp. 65-74
12. RUETHER K; VANDEPOL D; JAISSLE G; BERGER W; TORNOW RP; ZRENNER E
    RETINOSCHISISLIKE ALTERATIONS IN THE MOUSE EYE CAUSED BY GENE TARGETING OF THE NORRIE DISEASE GENE
    Investigative ophthalmology & visual science
    
    K. Ruether et al., "RETINOSCHISISLIKE ALTERATIONS IN THE MOUSE EYE CAUSED BY GENE TARGETING OF THE NORRIE DISEASE GENE", Investigative ophthalmology & visual science, 38(3), 1997, pp. 710-718
13. MARREN SE
    IDIOPATHIC PERIPHERAL VITREOUS MEMBRANES
    Optometry and vision science
    
    S.E. Marren, "IDIOPATHIC PERIPHERAL VITREOUS MEMBRANES", Optometry and vision science, 73(8), 1996, pp. 562-568
14. ANASTASI M; BRAI M; LAURICELLA M; GERACITANO R
    METHODOLOGICAL ASPECTS OF THE APPLICATION OF THE NAKA-RUSHTON EQUATION TO CLINICAL ELECTRORETINOGRAM
    Ophthalmic research
    
    M. Anastasi et al., "METHODOLOGICAL ASPECTS OF THE APPLICATION OF THE NAKA-RUSHTON EQUATION TO CLINICAL ELECTRORETINOGRAM", Ophthalmic research, 25(3), 1993, pp. 145-156
15. RUDANKO SL; FLAGE T; HANSEN E; ROSENBERG T; VIGGOSSON G; RIISE R
    VISUAL IMPAIRMENT IN NORDIC CHILDREN .5. X-LINKED JUVENILE RETINOSCHISIS
    Acta ophthalmologica
    
    S.L. Rudanko et al., "VISUAL IMPAIRMENT IN NORDIC CHILDREN .5. X-LINKED JUVENILE RETINOSCHISIS", Acta ophthalmologica, 71(5), 1993, pp. 586-589