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Publication Detail

Title: Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.

Authors: Truong, Brittany T; Yarza, Talitha K L; Bootpetch Roberts, Tori; Roberts, Susannah; Xu, Jonathan; Steritz, Matthew J; Tobias-Grasso, Celina A M; Azamian, Mahshid; Lalani, Seema R; Mohlke, Karen L; Lee, Nanette R; Cutiongco-de la Paz, Eva Maria; Reyes-Quintos, Maria Rina T; Santos-Cortez, Regie Lyn P; Chiong, Charlotte M

Published In Clin Genet, (2019 05)

Abstract: Abstract not available from PubMed.

PubMed ID: 30828794 Exiting the NIEHS site

MeSH Terms: No MeSH terms associated with this publication

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