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La ricerca find articoli where authors phrase all words ' VANDEPOL D' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 8 riferimenti
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    1. HOYNG CB; DEUTMAN AF; VANDEPOL D; KNOERS N; PINCKERS A; CREMERS FPM
      GENETIC-LINKAGE OF 2 DIFFERENT PHENOTYPES OF ROD AND CONE DYSTROPHY IN A FAMILY WITH PSEUDO-DOMINANT INHERITANCE TO 1P21-P13

      Investigative ophthalmology & visual science
    2. 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
    3. DENHOLLANDER A; VANDRIEL M; VANLIMPT V; DEKOK Y; VANDEPOL D; HOYNG C; DEUTMAN A; MORTON C; CREMERS F
      ISOLATION OF NOVEL RETINA-SPECIFIC, RETINAL-PIGMENT EPITHELIUM-SPECIFIC AND FETAL COCHLEA-SPECIFIC CDNA THROUGH SUPPRESSION SUBTRACTIVE HYBRIDIZATION

      American journal of human genetics
    4. CREMERS F; VANDEPOL D; ROZET JM; GERBER S; VANHAREN F; TIJMES N; BLANKENAGEL A; BERGEN A; KNOERS N; KREMER H; DAHL N; PINCKERS A; DEUTMAN A; KAPLAN J; HOYNG C
      LINKAGE ANALYSIS IN A FAMILY WITH PSEUDO-DOMINANTLY INHERITED CONE-ROD DYSTROPHY AND RETINITIS-PIGMENTOSA SUGGESTS THAT THE DEFECTS RESIDE IN THE STARGARDT-DISEASE GENE ABCR

      American journal of human genetics
    5. FUCHS S; VANDEPOL D; BEUDT U; KELLNER U; MEIRE F; BERGER W; GAL A
      3 NOVEL AND 2 RECURRENT MUTATIONS OF THE NORRIE DISEASE GENE IN PATIENTS WITH NORRIE SYNDROME

      Human mutation
    6. BERGER W; VANDEPOL D; BACHNER D; OERLEMANS F; WINKENS H; HAMEISTER H; WIERINGA B; HENDRIKS W; ROPERS HH
      AN ANIMAL-MODEL FOR NORRIE DISEASE (ND) - GENE TARGETING OF THE MOUSEND GENE

      Human molecular genetics
    7. VANDENHURK J; OERLEMANS F; VANDEPOL D; JAISSLE G; RUTHER K; ROPERS HH; WIERINGA B; CREMERS F; HENDRIKS W
      MATERNAL TRANSMISSION OF A CHOROIDEREMIA MUTATION IN MICE IS EMBRYONIC LETHAL

      American journal of human genetics
    8. BERGER W; DEROOS A; VANDEPOL D; VANDEVELDEVISSER S; SIMONS A; BOENDER V; ROSSUM L; CREMERS F; ROPERS HH
      EYE DISEASE LOCI IN XP - ISOLATION AND CHARACTERIZATION OF RESPONSIBLE GENES

      Cytogenetics and cell genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 21:58:54