Koc University Digital Collectionsmetadata only
Variations in multiple syndromic deafness genes mimic non-syndromic hearing loss
multidisciplinary sciences, copy-number variation; charge syndrome; noonan syndrome; pendred-syndrome; hypertrophic cardiomyopathy; waardenburg syndrome; diagnostic-criteria; mutation spectrum; slc26a4 mutations; kallmann-syndrome
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 934993
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.