[HTML][HTML] Research progress on incomplete partition type 3 inner ear malformation

K Xu, Y Xiao, J Luo, X Chao, R Wang, Z Fan… - European Archives of …, 2024 - Springer
Purpose This review aims to provides a comprehensive overview of the latest research
progress on IP-III inner ear malformation, focusing on its geneticbasis, imaging features …

Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia

F Almalki - Annals of Human Genetics, 2024 - Wiley Online Library
Congenital hearing loss is one of the most common sensory disabilities worldwide. The
genetic causes of hearing loss account for 50% of hearing loss. Genetic causes of hearing …