Showing results (161-170 of 194) with videos related to
Sort By:
Pageof 20
Molecular Cytogenetics|November 12, 2015
De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart diseaseYing Peng, Ruiyu Ma, Yingjie Zhou, et al.Journal of Human Genetics|January 13, 2017
Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated casesXiaomei Luo, Yongyi Zou, Bo Tan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 5, 2019
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromesDesheng Liang, David S Cram, Hu Tan, et al.Clinical Chemistry|November 8, 2014
Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)Weigang Lv, Xianda Wei, Ruolan Guo, et al.Journal of Radiation Research|August 12, 2004
The combination of suicide gene therapy and radiation enhances the killing of nasopharyngeal carcinoma xenographsJiahui Xia, Kun Xia, Yong Feng, et al.Clinical Chemistry|January 23, 2023
Evaluating the Clinical Utility of a Long-Read Sequencing-Based Approach in Prenatal Diagnosis of ThalassemiaQiaowei Liang, Jun He, Qing Li, et al.Cell Reports|November 19, 2023
A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorderHanzhe Kuang, Yunlong Li, Yixuan Wang, et al.Journal of Neurophysiology|January 17, 2024
Motor patterns of patients with spinal muscular atrophy suggestive of sensory and corticospinal contributions to the development of locomotor muscle synergiesVincent C K Cheung, Sophia C W Ha, Janet H Zhang-Lea, et al.Human Genetics|January 4, 2021
Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosisXin Chen, Wu Yin, Siyi Chen, et al.Frontiers in Genetics|July 24, 2023
Functional identification of two novel variants and a hypomorphic variant in <i>ASS1</i> from patients with Citrullinemia type IJing Liu, Zhongjie Wang, Huiming Yan, et al.Pageof 20