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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2007
Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: a case-control studyRui Yu, Xian-Ning Zhang, Xiao-Xiao Huang, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigreeChun-Yue Chen, Chen-Ming Xu, Zhen-Fang Du, et al.
Anatomical Record (Hoboken, N.J. : 2007)|January 21, 2012
The most common mutation of KRT9, c.C487T (p.R163W), in epidermolytic palmoplantar keratoderma in two large Chinese pedigreesWen-Ting Liu, Hai-Ping Ke, Yan Zhao, et al.
Journal of Zhejiang University. Science. B|February 7, 2009
Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophyYu-hua Liang, Xiao-ling Chen, Zhong-sheng Yu, et al.
Molecular Therapy. Nucleic Acids|September 10, 2018
CRISPR/Cas9-Mediated Treatment Ameliorates the Phenotype of the Epidermolytic Palmoplantar Keratoderma-like MouseXiao-Rui Luan, Xiao-Ling Chen, Yue-Xiao Tang, et al.
Zhonghua Yi Xue Za Zhi|October 31, 2013
[The clinical patterns and RET proto-oncogene identification of pheochromocytoma in 13 multiple endocrine neoplasia type 2A pedigrees]Xiao-ping Qi, Zhen-guang Chen, Hang-yang Jin, et al.
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