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Journal of Zhejiang University. Science. B|November 6, 2015
A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndromeYing Gao, Jin-li Bai, Xiao-yan Liu, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 11, 2011
[Genetic and clinical study on 17 cases of Angelman syndrome with deletion of 15q11-13]Jin-li Bai, Fang Song, Li-ping Zou, et al.Journal of Child Neurology|October 22, 2014
Association of copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein gene with the natural history in a Chinese spinal muscular atrophy cohortYu-jin Qu, Xiu-shan Ge, Jin-li Bai, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 13, 2009
[Molecular analysis of survival motor neuron gene in 338 suspicious children patients with spinal muscular atrophy]Fang Song, Yu-jin Qu, Li-ping Zou, et al.The Journal of Molecular Diagnostics : JMD|July 19, 2016
Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular AtrophyYu-Jin Qu, Jin-Li Bai, Yan-Yan Cao, et al.Journal of Zhejiang University. Science. B|May 6, 2014
Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 geneYan Li, Yu-jin Qu, Xue-mei Zhong, et al.Genetic Testing and Molecular Biomarkers|July 12, 2014
Subtle mutation detection of SMN1 gene in Chinese spinal muscular atrophy patients: implication of molecular diagnostic procedure for SMN1 gene mutationsJin-Li Bai, Yu-Jin Qu, Yan-Yan Cao, et al.Pageof 3