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Brain : a Journal of Neurology|June 26, 2018
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1Zhidong Cen, Zhengwen Jiang, You Chen, et al.Elife|July 24, 2015
Genomic variations of the mevalonate pathway in porokeratosisZhenghua Zhang, Caihua Li, Fei Wu, et al.Journal of Medical Genetics|November 12, 2018
Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagellaXiaojin He, Weiyu Li, Huan Wu, et al.Nature Communications|September 5, 2024
Effect of single blastocyst-stage versus single cleavage-stage embryo transfer on cumulative live births in women with good prognosis undergoing in vitro fertilization: Multicenter Randomized Controlled TrialXiang Ma, Jing Wang, Yuhua Shi, et al.Journal of Medical Genetics|February 14, 2020
Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAFMingrong Lv, Wangjie Liu, Wangfei Chi, et al.Pageof 7