00b6a2ad2e0d4f9ea5edc0b0eaaa935311813ab17de44890b57d282607e37e7d20f19d3ff1944656ac1d0bf8a12a535a54073a5255904d55b37ab80d35d982d25fa200fcc4e24b8ba591ccf224c9206b7912dc3c965c48758a647e136d4c0e308109b149a2dc41e3873474e2db7b076d86045018af6742698147df53a7f2498a8bd7a498c0254b61aceddbba61cef3208d9061bce6934d2ea56939e2ac9aa19ea934a2164f4e48c2b0e6d467eeeed6dac8c416d7224e4a77926c9c9041bf7259db74d6ce4e174d43a16a3d5084b292a5f536bd7754914aa0bbb65f1d25f4d3d4
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The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR GeneThe phenotypic spectrum of albinismClinical characteristics and natural history of rho-associated retinitis pigmentosa.The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous AlbinismCLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIESCRB1-associated retinal dystrophiesThe retinal pigmentation pathway in human albinismStargardt diseaseX-linked RetinoschisisThe Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D GeneGenotypic and Phenotypic Characteristics of CRB1-Associated Retinal DystrophiesQuality of life in patients with CRB1-associated retinal dystrophiesAltered organization of the visual cortex in FHONDA syndromeDefining inclusion criteria and endpoints for clinical trials
author
type
label
Maria M van Genderen
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lastName
van Genderen