Jiongjiong Hu

The predictive role of dual source CT for esophageal foreign bodies.

Zhaoxin Ma, Zhenghua Zhu, Wei Li, 2014, American journal of otolaryngology.

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Duan Ma, Zhaoxin Ma, Jiongjiong Hu, 2015, PloS one.

Grhl1 deficiency affects inner ear development in zebrafish.

Duan Ma, Zhaoxin Ma, Xu Wang, 2015, The International journal of developmental biology.

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss

Duan Ma, Zhaoxin Ma, Zhenghua Zhu, 2016, Journal of Translational Medicine.

Mutations in TOP2B cause autosomal‐dominant hereditary hearing loss via inhibition of the PI3K‐Akt signalling pathway

Duan Ma, Zhaoxin Ma, Jin Zhang, 2019, FEBS letters.

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish

Weidong Tian, Duan Ma, Xu Wang, 2015, PloS one.

Delayed repair of facial nerve trauma: an experimental study in guinea pigs

Liang Zhou, Zhaoxin Ma, Jiongjiong Hu, 2013, Acta oto-laryngologica.

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss

Fei Liu, Duan Ma, Zhaoxin Ma, 2016, Human molecular genetics.

Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss

Duan Ma, Zhaoxin Ma, Xu Wang, 2019, Clinical genetics.

Identification of ANLN as a new likely pathogenic gene of branchio‐otic syndrome in a three‐generation Chinese family

Zhaoxin Ma, Jiongjiong Hu, Wenjun Xia, 2018, Molecular genetics & genomic medicine.

New role of LRP5, associated with nonsyndromic autosomal‐recessive hereditary hearing loss

Duan Ma, Zhaoxin Ma, Xu Wang, 2017, Human mutation.

[Revision endoscopic sinus surgery and combined therapy for recurrent sinusitis].

Changqing Zhao, Zhenghua Zhu, Jiongjiong Hu, 2009, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.