Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'LINKED JUVENILE RETINOSCHISIS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 15 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Berinstein, DM; Hiraoka, M; Trese, MT; Shastry, BS
      Coats' disease and congenital retinoschisis in a single eye: A case reportand DNA analysis

      OPHTHALMOLOGICA
    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
    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
    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
    5. Shastry, BS; Hiraoka, M; Trese, MT
      Lack of association of the Norrie disease gene with retinoschisis phenotype

      JAPANESE JOURNAL OF OPHTHALMOLOGY
    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
    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
    8. Kelly, J; Maumenee, IH
      Hereditary macular diseases

      INTERNATIONAL OPHTHALMOLOGY CLINICS
    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
    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
    11. Weber, BHF
      Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula

      ACTA ANATOMICA
    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
    13. MARREN SE
      IDIOPATHIC PERIPHERAL VITREOUS MEMBRANES

      Optometry and vision science
    14. ANASTASI M; BRAI M; LAURICELLA M; GERACITANO R
      METHODOLOGICAL ASPECTS OF THE APPLICATION OF THE NAKA-RUSHTON EQUATION TO CLINICAL ELECTRORETINOGRAM

      Ophthalmic research
    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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 23:30:02