Hai-bo Li

Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV.

Yong Feng, L. Mei, Hongsheng Chen, 2014, Gene.

Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family

J. Yu, X. Liu, Jianguo Zhang, 2014, Journal of Human Genetics.

Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree.

Yan Yang, Lusi Zhang, Chun Ding, 2018, International journal of ophthalmology.

Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.

L. Mei, Chufeng He, Lu Jiang, 2017, International journal of pediatric otorhinolaryngology.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.