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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2009
Otosclerosis or congenital stapes ankylosis? The diagnostic role of genetic analysisSarah B Emery, Anna Meyer, Laura Miller, et al.
Biosecurity and Bioterrorism : Biodefense Strategy, Practice, and Science|September 3, 2011
Challenges in disposing of anthrax wasteAnn M Lesperance, Steve Stein, Jaki F Upton, et al.
Journal of Genetic Counseling|October 6, 2017
"My Plate is Full": Reasons for Declining a Genetic Evaluation of Hearing LossMarci M Lesperance, Erin Winkler, Tori L Melendez, et al.
Ophthalmic Genetics|November 12, 2010
Congenital cataracts in two siblings with Wolfram syndromeRebecca B Mets, Sarah B Emery, Marci M Lesperance, et al.
CANNT Journal = Journal ACITN|August 2, 2008
Are CSN and NKF-K/DOQI mineral metabolism guidelines for hemodialysis patients achievable? Results from a provincial renal programLori D Wazny, Colette B Raymond, Esther M Lesperance, et al.
Plos One|March 29, 2016
Assessing Conformance with Benford's Law: Goodness-Of-Fit Tests and Simultaneous Confidence IntervalsM Lesperance, W J Reed, M A Stephens, et al.
Ear and Hearing|April 14, 2026
Gene Therapy for Infants and Children With Otoferlin-Related Auditory Neuropathy Spectrum DisorderMarci M Lesperance, Jenna Devare, Ryan W McCreery, et al.
International Journal of Pediatric Otorhinolaryngology|July 20, 2010
Development of canal cholesteatoma in a patient with prenatal isotretinoin exposureKathryn M Van Abel, Marc E Nelson, Ryan M Collar, et al.
Head & Neck|June 4, 2013
Novel DICER1 mutation as cause of multinodular goiter in childrenIlaaf Darrat, Jirair K Bedoyan, Ming Chen, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 23, 2003
Mutations in the Wolfram syndrome type 1 gene (WFS1) define a clinical entity of dominant low-frequency sensorineural hearing lossMarci M Lesperance, James W Hall, Theresa B San Agustin, et al.
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