Xue Gao
10PUBLICATIONS
7CO-AUTHORS
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Publications (10)
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|Dec 06, 2025
A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss.Li-Ting Peng, Wei-Qian Wang, Sha-Sha Huang
|Nov 14, 2022
A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4.Kun Yang, Xi Wang, Wei-Qian Wang
|Aug 18, 2022
Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.Jie Wu, Zongfu Cao, Yu Su
|Jul 07, 2021
Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.Xue Gao, Pu Dai, Yong-Yi Yuan
|Aug 18, 2020
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation.Chang Guo, Sha-Sha Huang, Yong-Yi Yuan
|Aug 02, 2020
Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms.Xue Gao, Sha-Sha Huang, Shi-Wei Qiu
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