D. Han

发表

Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family

Q. Z. Li, Q. Wang, M. Guan, 2004, Journal of Medical Genetics.

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

S. Z. Yang, D. Yan, G. Feng, 2008, Clinical genetics.

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

S. Z. Yang, D. Yan, G. Feng, 2007, Clinical genetics.

LINC00673 rs11655237 C>T and susceptibility to Wilms tumor: A five‐center case–control study

Jing He, Jiwen Cheng, Jiao Zhang, 2019, The journal of gene medicine.

impairment in a large Chinese family Y-linked inheritance of non-syndromic hearing

Q. Wang, M. Guan, C. Lu, 2004 .

AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23–27.3

Q. Z. Li, S. Leal, J. Guan, 2005, Journal of Medical Genetics.

Clinical features of dementia with lewy bodies in 35 Chinese patients

Zhenfu Wang, D. Han, Zhong-bao Gao, 2014, Translational Neurodegeneration.

Case Report: Complete Maternal Uniparental Disomy of Chromosome 2 With a Novel UNC80 Splicing Variant c.5609-4G> A in a Chinese Patient With Infantile Hypotonia With Psychomotor Retardation and Characteristic Facies 2

D. Han, Xiaoze Li, Yiju Wei, 2021, Frontiers in Genetics.

A Case Report on Hemiplegia in a Patient with an Intracerebral Hemorrhage of the Basal Ganglia of the Corona Radiata Treated with Traditional Korean and Western Medicine

D. Han, A. Son, Hye-mi Jo, 2021, The Journal of Internal Korean Medicine.