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Pigment Cell & Melanoma Research|January 11, 2026
First Report of Oculocutaneous Albinism Type I Among Baka Pygmies From CameroonAlain Froment, Paul Verdu, Claudio Plaisant, et al.Ophthalmic Genetics|April 4, 2019
Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinismVincent Michaud, Sabine Defoort-Dhellemmes, Isabelle Drumare, et al.The Journal of Gene Medicine|April 5, 2020
Triple diagnosis of Wiedemann-Steiner, Waardenburg and DLG3-related intellectual disability association found by WES: A case reportThibaut Matis, Vincent Michaud, Julien Van-Gils, et al.European Journal of Human Genetics : EJHG|January 14, 2025
A patient with TPCN2-related hypopigmentation and ocular phenotypeCécile Courdier, Vincent Michaud, Modibo Diallo, et al.Platelets|April 5, 2020
A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodiesVincent Michaud, Mathieu Fiore, Valentine Coste, et al.Nature Communications|September 30, 2024
The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinismDavid J Green, Vincent Michaud, Eulalie Lasseaux, et al.Journal of Medical Genetics|July 17, 2023
A multilayered approach to the analysis of genetic data from individuals with suspected albinismPanagiotis I Sergouniotis, Vincent Michaud, Eulalie Lasseaux, et al.Pigment Cell & Melanoma Research|January 19, 2018
Molecular characterization of a series of 990 index patients with albinismEulalie Lasseaux, Claudio Plaisant, Vincent Michaud, et al.Pigment Cell & Melanoma Research|May 9, 2024
Genotypic spectrum of albinism in MaliModibo Diallo, Ousmane Sylla, Mohamed Kole Sidibé, et al.Human Genetics|January 21, 2021
A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrumAngèle Tingaud-Sequeira, Aurélien Trimouille, Manju Salaria, et al.Pageof 3