Deep Blue: Browsing by Author "Cremers, Frans P.M."

Now showing items 1-2 of 2

Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response

Wissinger, Bernd; Schaich, Simone; Baumann, Britta; Bonin, Michael; Jägle, Herbert; Friedburg, Christoph; Varsányi, Balázs; Hoyng, Carel B.; Dollfus, Hélène; Heckenlively, John R.; Rosenberg, Thomas; Rudolph, Günter; Kellner, Ulrich; Salati, Roberto; Plomp, Astrid; De Baere, Elfride; Andrassi‐darida, Monika; Sauer, Alexandra; Wolf, Christiane; Zobor, Ditta; Bernd, Antje; Leroy, Bart P.; Enyedi, Péter; Cremers, Frans P.M.; Lorenz, Birgit; Zrenner, Eberhart; Kohl, Susanne (Wiley Subscription Services, Inc., A Wiley Company, 2011-12)

(436.7KB) (558.6KB)
Screening of a Large Cohort of L eber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA 5 Mutations and New Genotype–Phenotype Correlations

Mackay, Donna S.; Borman, Arundhati Dev; Sui, Ruifang; Born, L. Ingeborgh; Berson, Eliot L.; Ocaka, Louise A.; Davidson, Alice E.; Heckenlively, John R.; Branham, Kari; Ren, Huanan; Lopez, Irma; Maria, Maleeha; Azam, Maleeha; Henkes, Arjen; Blokland, Ellen; Andreasson, Sten; Baere, Elfride; Bennett, Jean; Chader, Gerald J.; Berger, Wolfgang; Golovleva, Irina; Greenberg, Jacquie; Hollander, Anneke I.; Klaver, Caroline C.W.; Klevering, B. Jeroen; Lorenz, Birgit; Preising, Markus N.; Ramesar, Raj; Roberts, Lisa; Roepman, Ronald; Rohrschneider, Klaus; Wissinger], Bernd; Qamar, Raheel; Webster, Andrew R.; Cremers, Frans P.M.; Moore, Anthony T.; Koenekoop, Robert K. (Wiley Periodicals, Inc., 2013-11)

(878.9KB)