Repository of Research and Investigative Information

Repository of Research and Investigative Information

Ilam University of Medical Sciences

Items where Author is "Cengiz, F. B."

Sun Sep 25 15:39:50 2022
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(2013) Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE). Plos One. ISSN 19326203 (ISSN)

This list was generated on Sun Sep 25 12:22:07 2022 +0330.