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Journal of Zhejiang University. Science. B|February 8, 2008
Mitochondrion and its related disorders: making a comebackXian-ning Zhang, Ming Qi
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|February 10, 2007
[Research advances in human mitochondrial DNA with aging and degenerative diseases]Dong-Dong Ti, Xian-Ning Zhang
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|October 11, 2005
[PCR products with heterozygous mutations containing two types of heteroduplexes]Xian-ning Zhang, Xin-hui He, Ji-cheng Li
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 10, 2004
[Present status of the molecular genetics in epidermolytic palmoplantar keratoderma]Xian-ning Zhang, Wei Mao, Xin-hui He, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 7, 2003
[Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene]Xian-ning Zhang, Lie-min Ruan, Yan-ping Le, et al.
Journal of Cellular and Molecular Medicine|December 21, 2005
Evaluation of the ELOVL4 gene in a Chinese family with autosomal dominant STGD3-like macular dystrophyZheng Lai, Xian-Ning Zhang, Wei Zhou, et al.
American Journal of Ophthalmology|June 13, 2006
Recurrent FBN1 mutation (R62C) in a Chinese family with isolated ectopia lentisRui Yu, Zheng Lai, Wei Zhou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2004
102T/C SNP in the 5-hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern Han Chinese populations: lack of associationXian-Ning Zhang, San-Duo Jiang, Xin-Hui He, et al.
Frontiers in Bioengineering and Biotechnology|May 13, 2022
Recent Advances and Perspective of Nanotechnology-Based Implants for Orthopedic ApplicationsMing-Qi Chen
International Journal of Ophthalmology|May 4, 2012
Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutationLei Shu, Yong-Ming Zhang, Xiao-Xiao Huang, et al.
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