Items where Author is "Alimadadi, H."
 | Up a level |
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 1.
Article
(2017) SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis. International Journal of Pediatric Otorhinolaryngology. pp. 122-126. ISSN 0165-5876