Results 151 to 160 of about 431,670 (160)

Localization of a Gene (CORD7) for a Dominant Cone-Rod Dystrophy to Chromosome 6q

American Journal of Human Genetics, 1998
Anthony T Moore, Cheryl Y Gregory-Evans, Alan C Bird   +2 more
exaly  

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy

Documenta Ophthalmologica, 2012
Bernd Wissinger, Kari Branham, Naheed W Khan   +2 more
exaly  

Rod and Cone Photoreceptor Function in Patients with Cone Dystrophy

Investigative Ophthalmology and Visual Science, 2004
William H Seiple, Vivienne C Greenstein, Donald C Hood   +2 more
exaly  

SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa

Ophthalmic Genetics, 2016
Robert Koenekoop, David B McGuigan, Artur V Cideciyan   +2 more
exaly  

Pediatric Cone-Rod Dystrophy with High Myopia and Nystagmus Suggests Recessive PROM1 Mutations.

Ophthalmic Genetics, 2015
Hanno J Bolz, Arif Khan
exaly  

Progressive cone-rod dystrophy and high myopia in a Finnish family

Acta Ophthalmologica, 1989
Kaija Tuppurainen, Maija Mäntyjärvi, K Tuppurainen   +2 more
exaly  

A novel recessive GUCY2D mutation causing cone–rod dystrophy and not Leber's congenital amaurosis

European Journal of Human Genetics, 2010
Aslıhan Tolun, Sibel Aylin Uğur
exaly  

Mizuo‐Nakamura phenomenon in cone‐rod dystrophy

Australasian journal of optometry, The, 2017
Itika Garg, Neha Goel
exaly  

Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands

Experimental Eye Research, 2016
Qingjiong Zhang, Yan Xu, Xiangming Guo
exaly  

Cone Dystrophy/Cone-Rod Dystrophy

2022
exaly