L. Xie

Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I

G. He, Yongjing Lai, Zhijie Niu, 2022, Molecular genetics & genomic medicine.

High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder

L. Lan, Z. Yin, J. Guan, 2016, Clinical genetics.

Histone acetylation in refractory sudden sensorineural hearing loss patients after intratympanic methylprednisolone perfusion

J. Hou, H. Qi, W. She, 2019, The Journal of Laryngology & Otology.

[Classification of sudden deafness prognosis based on deep learning method].

D. Bing, J. Ying, L. Lan, 2018, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.