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Publications by Marci M. Lesperance
A Comprehensive Review of Reported Heritable Noggin-Associated Syndromes and Proposed Clinical Utility of One Broadly Inclusive Diagnostic Term: NOG-related-symphalangism Spectrum Disorder (NOG-SSD)
Human Mutation
Genetics
Phenotypic Characterization of Hereditary Hearing Impairment Linked to DFNA25
Archives of Otolaryngology–Head & Neck Surgery
Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss
Archives of Otolaryngology–Head & Neck Surgery
No Association betweenDFNA6 and Pro250Arg Mutation inFGFR3
American Journal of Medical Genetics
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