نتائج البحث - Jack Weeda
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1
Risk factors for development and progression of diabetic retinopathy in Dutch patients with type 1 diabetes mellitus حسب Vivian Schreur, Freekje van Asten, Heijan Ng, Jack Weeda, J.M.M. Groenewoud, Cees J. Tack, Carel B. Hoyng, Eiko K. de Jong, Caroline C. W. Klaver, B. Jeroen Klevering
منشور في 2018Artigo -
2
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants حسب Hedwig M. Velde, Janine Reurink, Sebastian Held, Catherina H. Z. Li, Suzanne Yzer, Jaap Oostrik, Jack Weeda, Lonneke Haer‐Wigman, Helger G. Yntema, Susanne Roosing, Laurenz Pauleikhoff, Clemens Lange, Laura Whelan, Adrian Dockery, Julia Zhu, David Keegan, G. Jane Farrar, Hannie Kremer, Cris Lanting, Markus Daμμe, Ronald J. E. Pennings
منشور في 2022Artigo -
3
MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse حسب Mieke Wesdorp, Silvia Murillo‐Cuesta, Theo Peters, Adelaida M. Celaya, Anne M.M. Oonk, Margit Schraders, Jaap Oostrik, Elena Gómez-Rosas, Andy J. Beynon, Bas P. Hartel, Kees Okkersen, Hans J. P. M. Koenen, Jack Weeda, Stefan H. Lelieveld, Nicol C. Voermans, Irma Joosten, Carel B. Hoyng, Peter Lichtner, Henricus P. M. Kunst, Ilse Feenstra, Suzanne E. de Bruijn, R.J.C. Admiraal, Helger G. Yntema, Erwin van Wijk, Ignacio del Castillo, Pau Serra, Isabel Varela‐Nieto, Ronald J. E. Pennings, Hannie Kremer, M. F. van Dooren, H.H.W. de Gier, E. H. Hoefsloot, Marc P. van der Schroeff, Sarina G. Kant, Liselotte J. C. Rotteveel, Suzanna G.M. Frints, J.R. Hof, Robert J. Stokroos, Els K. Vanhoutte, R.J.C. Admiraal, Ilse Feenstra, Hannie Kremer, Henricus P. M. Kunst, Ronald J. E. Pennings, Helger G. Yntema, A.J. van Essen, Rolien H. Free, J.S. Klein-Wassink
منشور في 2018Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Medicine
Albuminuria
Anatomy
Audiology
Blood pressure
Body mass index
Cell cycle
Cochlea
Computational biology
Diabetes mellitus
Diabetic retinopathy
Endocrinology
Exome sequencing
Hair cell
Hearing loss
Human genetics
Inner ear
Internal medicine
Molecular medicine
Mutation
Ophthalmology
Organ of Corti
Pathology
Phenotype
Proportional hazards model
Retinitis pigmentosa
Retinopathy