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

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Bibliografiske detaljer
Udgivet i:Clin Genet
Main Authors: Truong, Brittany T., Yarza, Talitha Karisse L., Roberts, Tori Bootpetch, Roberts, Susannah, Xu, Jonathan, Steritz, Matthew J., Tobias-Grasso, Celina Ann 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.
Format: Artigo
Sprog:Inglês
Udgivet: 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6499369/
https://ncbi.nlm.nih.gov/pubmed/30828794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.13515
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