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Current Opinion in Neurology|September 22, 2007
Neuropathies associated with conduction blockRichard Alan LewisHuman Genetics|February 1, 2007
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14Wojciech Wiszniewski, Richard Alan Lewis, James R LupskiAmerican Journal of Rhinology|February 8, 2007
Rhinologic manifestations of ectodermal dysplasiaUmang Mehta, Joseph Brunworth, Richard Alan Lewis, et al.Annals of Medicine|July 1, 2004
Triallelic inheritance: a bridge between Mendelian and multifactorial traitsErica R Eichers, Richard Alan Lewis, Nicholas Katsanis, et al.Journal of Medical Genetics|May 15, 2017
Genetic causes of optic nerve hypoplasiaChun-An Chen, Jiani Yin, Richard Alan Lewis, et al.Molecular Genetics and Metabolism|April 13, 2012
30-year follow-up of a patient with classic citrullinemiaNicola Brunetti-Pierri, Kerri M Lamance, Richard Alan Lewis, et al.Middle East African Journal of Ophthalmology|March 10, 2016
Novel Mutations in Two Saudi Patients with Congenital Retinal DystrophyLeen Abu Safieh, Humoud M Al-Otaibi, Richard Alan Lewis, et al.The International Journal of Neuroscience|March 18, 2014
Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 geneAziz Shaibani, Lee-Jun Wong, Victor Wei Zhang, et al.American Journal of Medical Genetics. Part A|October 18, 2008
Neuroimaging aspects of Aicardi syndromeBobbi Hopkins, V Reid Sutton, Richard Alan Lewis, et al.Ophthalmic Genetics|December 29, 2004
Molecular basis of Peters anomaly in Saudi ArabiaDeepak Edward, Ali Al Rajhi, Richard Alan Lewis, et al.Pageof 6