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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|December 28, 2012
Molecular genetic testing for mitochondrial disease: from one generation to the nextElizabeth McCormick, Emily Place, Marni J FalkHuman Mutation|April 13, 2019
Characterizing variants of unknown significance in rhodopsin: A functional genomics approachAliete Wan, Emily Place, Eric A Pierce, et al.Ophthalmic Genetics|August 16, 2024
A novel homozygous nonsense variant in <i>CABP4</i> causing stationary cone/rod synaptic dysfunctionBlake M Hauser, Emily Place, Rachel Huckfeldt, et al.Plos One|November 13, 2015
Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis PigmentosaKinga M Bujakowska, Joseph White, Emily Place, et al.Journal of Pediatric Hematology/Oncology|May 8, 2007
Successful plasmapheresis for extreme hyperbilirubinemia caused by acute Epstein-Barr virusEmily Place, Judith E Wenzel, Ramalingam Arumugam, et al.Clinical Nephrology|March 24, 2016
Claudin 19-based familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a sibling pairSheena Sharma, Emily Place, Katherine Lord, et al.Retinal Cases & Brief Reports|August 25, 2022
WIDEFIELD SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN WAGNER SYNDROMEIsaac D Bleicher, Itika Garg, Sandra Hoyek, et al.Molecular Genetics and Metabolism|August 8, 2013
Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolitesColleen Clarke, Rui Xiao, Emily Place, et al.Genes|October 6, 2017
The Genetic Basis of Pericentral Retinitis Pigmentosa-A Form of Mild Retinitis PigmentosaJason Comander, Carol Weigel-DiFranco, Matthew Maher, et al.Discovery Medicine|February 29, 2012
Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataractsSamantha A Schrier, Lee-Jun Wong, Emily Place, et al.Pageof 4