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Retina (Philadelphia, Pa.)|August 23, 2018
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHYXuan Zou, Qing Fu, Sha Fang, et al.Investigative Ophthalmology & Visual Science|February 26, 2015
Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patientsJason Salvo, Vera Lyubasyuk, Mingchu Xu, et al.Human Genetics|July 29, 2015
Mutations in human IFT140 cause non-syndromic retinal degenerationMingchu Xu, Lizhu Yang, Feng Wang, et al.Human Mutation|December 15, 2015
ADIPOR1 Is Mutated in Syndromic Retinitis PigmentosaMingchu Xu, Aiden Eblimit, Jing Wang, et al.Nature Communications|August 19, 2021
Single-cell evaluation reveals shifts in the tumor-immune niches that shape and maintain aggressive lesions in the breastVidya C Sinha, Amanda L Rinkenbaugh, Mingchu Xu, et al.The Journal of Molecular Diagnostics : JMD|September 14, 2016
Improved Diagnosis of Inherited Retinal Dystrophies by High-Fidelity PCR of ORF15 followed by Next-Generation SequencingJianli Li, Jia Tang, Yanming Feng, et al.Genome Research|February 26, 2016
Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genesLi Zhao, Yiyun Chen, Amol Onkar Bajaj, et al.Scientific Reports|August 3, 2017
The phenotypic variability of HK1-associated retinal dystrophyZhisheng Yuan, Baiyu Li, Mingchu Xu, et al.Molecular Genetics and Metabolism Reports|November 23, 2016
Diagnosis of a mild peroxisomal phenotype with next-generation sequencingMeredith J Ventura, Dianna Wheaton, Mingchu Xu, et al.Journal of Medical Genetics|September 16, 2016
CEP78 is mutated in a distinct type of Usher syndromeQing Fu, Mingchu Xu, Xue Chen, et al.Pageof 4