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Current Opinion in Genetics & Development|June 30, 2020
The frontiers of sequencing in undiagnosed neurodevelopmental diseasesHane Lee, Stanley F NelsonAnnals of the New York Academy of Sciences|August 8, 2015
Clinical exome sequencing in neurogenetic and neuropsychiatric disordersBrent L Fogel, Hane Lee, Samuel P Strom, et al.Archives of Neurology|May 16, 2007
A new episodic ataxia syndrome with linkage to chromosome 19q13Kevin A Kerber, Joanna C Jen, Hane Lee, et al.Headache|December 18, 2007
Phenotypic and genetic analysis of a large family with migraine-associated vertigoHane Lee, Joanna C Jen, Yoon-Hee Cha, et al.Human Mutation|November 9, 2004
A novel mutation in KCNA1 causes episodic ataxia without myokymiaHane Lee, Hui Wang, Joanna C Jen, et al.Human Molecular Genetics|February 7, 2014
Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivationHane Lee, Meng-chin A Lin, Harley I Kornblum, et al.Neurogenetics|July 5, 2007
Association of progesterone receptor with migraine-associated vertigoHane Lee, Lauren Sininger, Joanna C Jen, et al.Molecular Genetics and Metabolism Reports|April 14, 2020
Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndromeShahram Yazdani, Anish Badjatiya, Naghmeh Dorrani, et al.Annals of Neurology|July 17, 2016
Truncating mutations in APP cause a distinct neurological phenotypeSteven Klein, Alexander Goldman, Hane Lee, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 11, 2014
Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratorySamuel P Strom, Hane Lee, Kingshuk Das, et al.Pageof 32