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Results: 1-8 |
Results: 8
GENETIC-LINKAGE OF 2 DIFFERENT PHENOTYPES OF ROD AND CONE DYSTROPHY IN A FAMILY WITH PSEUDO-DOMINANT INHERITANCE TO 1P21-P13
Authors: HOYNG CB DEUTMAN AF VANDEPOL D KNOERS N PINCKERS A CREMERS FPM
Citation: Cb. Hoyng et al., 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, 38(4), 1997, pp. 3690-3690
RETINOSCHISISLIKE ALTERATIONS IN THE MOUSE EYE CAUSED BY GENE TARGETING OF THE NORRIE DISEASE GENE
Authors: RUETHER K VANDEPOL D JAISSLE G BERGER W TORNOW RP ZRENNER E
Citation: 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
ISOLATION OF NOVEL RETINA-SPECIFIC, RETINAL-PIGMENT EPITHELIUM-SPECIFIC AND FETAL COCHLEA-SPECIFIC CDNA THROUGH SUPPRESSION SUBTRACTIVE HYBRIDIZATION
Authors: DENHOLLANDER A VANDRIEL M VANLIMPT V DEKOK Y VANDEPOL D HOYNG C DEUTMAN A MORTON C CREMERS F
Citation: A. Denhollander et al., ISOLATION OF NOVEL RETINA-SPECIFIC, RETINAL-PIGMENT EPITHELIUM-SPECIFIC AND FETAL COCHLEA-SPECIFIC CDNA THROUGH SUPPRESSION SUBTRACTIVE HYBRIDIZATION, American journal of human genetics, 61(4), 1997, pp. 1357-1357
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
Authors: 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
Citation: F. Cremers et al., 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, 61(4), 1997, pp. 1930-1930
3 NOVEL AND 2 RECURRENT MUTATIONS OF THE NORRIE DISEASE GENE IN PATIENTS WITH NORRIE SYNDROME
Authors: FUCHS S VANDEPOL D BEUDT U KELLNER U MEIRE F BERGER W GAL A
Citation: S. Fuchs et al., 3 NOVEL AND 2 RECURRENT MUTATIONS OF THE NORRIE DISEASE GENE IN PATIENTS WITH NORRIE SYNDROME, Human mutation, 8(1), 1996, pp. 85-88
AN ANIMAL-MODEL FOR NORRIE DISEASE (ND) - GENE TARGETING OF THE MOUSEND GENE
Authors: BERGER W VANDEPOL D BACHNER D OERLEMANS F WINKENS H HAMEISTER H WIERINGA B HENDRIKS W ROPERS HH
Citation: W. Berger et al., AN ANIMAL-MODEL FOR NORRIE DISEASE (ND) - GENE TARGETING OF THE MOUSEND GENE, Human molecular genetics, 5(1), 1996, pp. 51-59
MATERNAL TRANSMISSION OF A CHOROIDEREMIA MUTATION IN MICE IS EMBRYONIC LETHAL
Authors: VANDENHURK J OERLEMANS F VANDEPOL D JAISSLE G RUTHER K ROPERS HH WIERINGA B CREMERS F HENDRIKS W
Citation: J. Vandenhurk et al., MATERNAL TRANSMISSION OF A CHOROIDEREMIA MUTATION IN MICE IS EMBRYONIC LETHAL, American journal of human genetics, 57(4), 1995, pp. 274-274
EYE DISEASE LOCI IN XP - ISOLATION AND CHARACTERIZATION OF RESPONSIBLE GENES
Authors: BERGER W DEROOS A VANDEPOL D VANDEVELDEVISSER S SIMONS A BOENDER V ROSSUM L CREMERS F ROPERS HH
Citation: W. Berger et al., EYE DISEASE LOCI IN XP - ISOLATION AND CHARACTERIZATION OF RESPONSIBLE GENES, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 175-175
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