Min Liu

发表

A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

Yong Feng, Xue Gao, Yongyi Yuan, 2021, BMC Medical Genomics.

A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4

Xue Gao, Yongyi Yuan, D. Kang, 2022, Molecular genetics & genomic medicine.

Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations

Yanhui Lu, Xue Gao, P. Dai, 2023, Medicine.