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Showing results (21-30 of 22) with videos related to

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Clinical Genetics|July 29, 2018
Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophiesN Patel, H Alkuraya, S S Alzahrani, et al.
European Journal of Neurology|September 12, 2019
Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelinationV Chelban, M Alsagob, K Kloth, et al.
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Showing results (21-30 of 22) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 22 results.
Clinical Genetics|July 29, 2018
Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophiesN Patel, H Alkuraya, S S Alzahrani, et al.
European Journal of Neurology|September 12, 2019
Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelinationV Chelban, M Alsagob, K Kloth, et al.
Pageof 3