Search Results - Weisschuh, Nicole
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Optic disc drusen and family history of Glaucoma: results of a patient-directed survey by Gramer, Gwendolyn (Author) , Gramer, Eugen (Author) , Weisschuh, Nicole (Author) ,
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2
Homozygosity mapping and whole-genome sequencing reveals a deep intronic PROM1 mutation causing cone-rod dystrophy by pseudoexon activation by Weik, Anja Kathrin (Author) , Rohrschneider, Klaus (Author) , Strom, Tim M. (Author) , Glöckle, Nicola (Author) , Kohl, Susanne (Author) , Wissinger, Bernd (Author) , Weisschuh, Nicole (Author) ,
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Mutation detection in patients with retinal dystrophies using targeted next generation sequencing by Weisschuh, Nicole (Author) , Rohrschneider, Klaus (Author) ,
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Mutations in RAB28, encoding a farnesylated small GTPase: are associated with autosomal-recessive cone-rod dystrophy by Roosing, Susanne (Author) , Rohrschneider, Klaus (Author) , Beryozkin, Avigail (Author) , Sharon, Dror (Author) , Weisschuh, Nicole (Author) , Staller, Jennifer (Author) , Kohl, Susanne (Author) , Zelinger, Lina (Author) , Peters, Theo A. (Author) , Neveling, Kornelia (Author) , Strom, Tim M. (Author) , van den Born, L. Ingeborgh (Author) , Hoyng, Carel B. (Author) , Klaver, Caroline C. W. (Author) , Roepman, Ronald (Author) , Wissinger, Bernd (Author) , Banin, Eyal (Author) , Cremers, Frans P. M. (Author) , den Hollander, Anneke I. (Author) ,
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5
Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma by Wolf, Christiane (Author) , Gramer, Eugen (Author) , Müller-Myhsok, Bertram (Author) , Pasutto, Francesca (Author) , Gramer, Gwendolyn (Author) , Wissinger, Bernd (Author) , Weisschuh, Nicole (Author) ,
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