Disease: Ossicular Malformations- familial
- A novel intronic TCOF1 pathogenic variant in a Chinese family with Treacher Collins syndrome
- Anatomical measurement of the ossicles in patients with congenital aural atresia and stenosis
- Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatment
- Branchio-oto-renal syndrome or branchio-oto syndrome: the clinical and genetic analysis in five Chinese families
- Congenital stapes ankylosis associated with another ossicular chain anomaly: surgical results in 30 ears
- Endoscopic Ossiculoplasty for the Management of Isolated Congenital Ossicular Chain Malformation: Surgical Results in 16 Ears
- Fallopian canal stapedotomy in congenital stapes fixation with aberrant facial nerve
- Hearing Loss in Adults: Differential Diagnosis and Treatment
- Hearing outcomes in functional surgery for middle ear malformations
- Juvenile otosclerosis and congenital stapes footplate fixation. A systematic review and meta-analysis of surgical outcomes and management
- Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update
- Middle ear malformations in identical twins
- Molecular Genetic Etiology and Revisiting the Middle Ear Surgery Outcomes of Branchio-Oto-Renal Syndrome: Experience in a Tertiary Referral Center
- Novel syndrome with conductive hearing loss and congenital glaucoma in three generations
- Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutation
- Rare and unusual case of familial focal dermal hypoplasia (Goltz syndrome) presenting to otolaryngology in the UK
- SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans
- Stapedectomy in Teunissen-Cremers Syndrome: Intraoperative Findings and Hearing Outcomes