Showing 1 — 20 of 645
SORT: Best Match Most Recent Oldest
VIEW: Basic | Expanded
  • Brief Report August 01, 2014

    Aman Chandra, MRCSEd, FRCOphth, PhD; Gavin Arno, PhD; Kathleen Williamson, PhD; Panagiotis I. Sergouniotis, PhD; Markus N. Preising, PhD; David G. Charteris, FRCOphth; Dorothy A. Thompson, PhD; Graham E. Holder, PhD; Arundhati Dev Borman, MRCOphth; Indran Davagnanam, FRCR; Andrew R. Webster, FRCOphth; Birgit Lorenz, FEBO; David R. FitzPatrick, FRCP (Edin); Anthony T. Moore, FRCOphth
    TOPICS: phenotype, mutation, genetics, microcornea

    JAMA Ophthalmol. 2014; 132(8):996-1001. doi: 10.1001/jamaophthalmol.2014.940

    Includes: Supplemental Content
  • Ophthalmic Molecular Genetics November 01, 2012

    Alejandro Estrada-Cuzcano, BSc; Robert K. Koenekoop, MD, PhD; Audrey Senechal, PhD; Elfride B. W. De Baere, MD, PhD; Thomy de Ravel, MD, PhD; Sandro Banfi, MD; Susanne Kohl, MD; Carmen Ayuso, MD, PhD; Dror Sharon, PhD; Carel B. Hoyng, MD; Christian P. Hamel, MD, PhD; Bart P. Leroy, MD, PhD; Carmela Ziviello, BS; Irma Lopez, PhD; Alexandre Bazinet, MD; Bernd Wissinger, PhD; Ieva Sliesoraityte, MD; Almudena Avila-Fernandez, PhD; Karin W. Littink, MD, PhD; Enzo M. Vingolo, MD; Sabrina Signorini, MD, PhD; Eyal Banin, MD, PhD; Liliana Mizrahi-Meissonnier, PhD; Eberhard Zrenner, MD; Ulrich Kellner, MD; Rob W. J. Collin, PhD; Anneke I. den Hollander, PhD; Frans P. M. Cremers, PhD; B. Jeroen Klevering, MD, PhD
    TOPICS: phenotype, mutation, bardet-biedl syndrome, retinitis pigmentosa

    Arch Ophthalmol. 2012; 130(11):1425-1432. doi: 10.1001/archophthalmol.2012.2434