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Human Mutation|April 10, 2013
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnosticsBirgit Sikkema-Raddatz, Lennart F Johansson, Eddy N de Boer, et al.
Journal of Neurotrauma|November 17, 2020
Imaging Markers for the Characterization of Gray and White Matter Changes from Acute to Chronic Stages after Experimental Traumatic Brain InjuryMichel R T Sinke, Willem M Otte, Anu E Meerwaldt, et al.
Molecular Brain|January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
Clinical Chemistry|May 26, 2018
Genetic Screening Test to Detect Translocations in Acute Leukemias by Use of Targeted Locus AmplificationMohamed Z Alimohamed, Lennart F Johansson, Eddy N de Boer, et al.
Clinical Epigenetics|February 16, 2024
Epigenome-wide association study of dietary fatty acid intakeJulia Lange de Luna, Aayah Nounu, Sonja Neumeyer, et al.
Neurology|March 13, 2002
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysisB P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, et al.
Archives of Neurology|January 11, 2007
The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch populationNadia A Sutedja, Richard J Sinke, Paul W J Van Vught, et al.
Neuromuscular Disorders : NMD|April 10, 2013
Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in The NetherlandsXenia L Stalpers, Aad Verrips, Bwee Tien Poll-The, et al.
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