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Current Opinion in Pediatrics|August 24, 2016
Navigating genetic diagnostics in patients with hearing lossChristina M Sloan-Heggen, Richard J H SmithAmerican Journal of Medical Genetics. Part A|March 9, 2023
An atypically mild case of ethylmalonic encephalopathy with pathogenic ETHE1 variantDaniel T Kashima, Christina M Sloan-Heggen, Rachel J Gottlieb-Smith, et al.Hearing Research|February 19, 2017
Genetic variants in the peripheral auditory system significantly affect adult cochlear implant performanceA Eliot Shearer, Robert W Eppsteiner, Kathy Frees, et al.The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.American Journal of Human Genetics|September 25, 2018
Genomic Landscape and Mutational Signatures of Deafness-Associated GenesHela Azaiez, Kevin T Booth, Sean S Ephraim, et al.Ophthalmic Genetics|April 14, 2020
Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing lossHeather A Stiff, Christina M Sloan-Heggen, Ashley Ko, et al.Human Genetics|March 13, 2016
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing lossChristina M Sloan-Heggen, Amanda O Bierer, A Eliot Shearer, et al.Journal of Medical Genetics|October 9, 2015
Characterising the spectrum of autosomal recessive hereditary hearing loss in IranChristina M Sloan-Heggen, Mojgan Babanejad, Maryam Beheshtian, et al.Pageof 1