Showing results (61-70 of 132) with videos related to

Sort By:
Pageof 14
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 18, 2019
Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South ChinaMin Chen, Chao Chen, Yingting Li, et al.
Translational Lung Cancer Research|January 9, 2026
A study protocol of a single-arm, prospective, open-label, non-controlled, phase II study of neoadjuvant BL-B01D1 combined with aumolertinib in resectable stage II-IIIB non-small cell lung cancer patients with EGFR mutationYue Chen, Jiandong Mei, Ge Gao, et al.
Materials Science & Engineering. C, Materials for Biological Applications|October 27, 2021
Chondrocyte-laden GelMA hydrogel combined with 3D printed PLA scaffolds for auricle regenerationPei Tang, Ping Song, Zhiyu Peng, et al.
Hemoglobin|April 1, 2021
Report of Two Novel Thalassemia Variants, HBB: c.181delG and HBA1: c.121_126delAAGACC, in Chinese IndividualsXinping Chen, Zhangli Lin, Junjie Hu, et al.
Journal of Thoracic Disease|July 13, 2018
Next generation sequencing-based molecular profiling of lung adenocarcinoma using pleural effusion specimensLiping Liu, Di Shao, Qiuhua Deng, et al.
BMC Genomics|November 20, 2014
Transcriptome profiling shows gene regulation patterns in a flavonoid pathway in response to exogenous phenylalanine in Boesenbergia rotunda cell cultureNoor Diyana Md-Mustafa, Norzulaani Khalid, Huan Gao, et al.
Biotechniques|January 31, 2020
Noninvasive prenatal diagnosis of hemophilia A by a haplotype-based approach using cell-free fetal DNAChao Chen, Jun Sun, Yun Yang, et al.
BMC Medical Genomics|November 18, 2023
Accuracy and depth evaluation of clinical low pass genome sequencing in the detection of mosaic aneuploidies and CNVsYanqiu Liu, Shengju Hao, Xueqin Guo, et al.
Frontiers in Genetics|March 5, 2026
Novel LARS2 variants in patients with Perrault syndrome: expanding the genetic spectrum and phenotypic heterogeneityZibin Lin, Jiale Xiang, Xiangzhong Sun, et al.
Clinical Chemistry|May 19, 2023
The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing DataJiale Xiang, Jiguang Peng, Xiangzhong Sun, et al.
Pageof 14