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Cancer Discovery|March 1, 2020
Plasma DNA End-Motif Profiling as a Fragmentomic Marker in Cancer, Pregnancy, and TransplantationPeiyong Jiang, Kun Sun, Wenlei Peng, et al.
Molecular Genetics & Genomic Medicine|May 1, 2020
The KLHL40 c.1516A>C is a Chinese-specific founder mutation causing nemaline myopathy 8: Report of six patients with pre- and postnatal phenotypesKit San Yeung, Florrie N Y Yu, Cheuk Wing Fung, et al.
BMC Medical Genomics|October 26, 2018
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
Nature Methods|September 1, 2022
Antibody stabilization for thermally accelerated deep immunostainingHei Ming Lai, Yumi Tang, Zachary Y H Lau, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 26, 2023
Combining Transoral Nasopharyngeal Brush and Plasma Epstein-Barr Virus DNA in Detecting Locally Recurrent Nasopharyngeal CarcinomaRonald Lai, David Chun Man Yeung, Zenon Wing Chi Yeung, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 28, 2012
Pathway analyses identify TGFBR2 as potential breast cancer susceptibility gene: results from a consortium study among AsiansXiangyu Ma, Alicia Beeghly-Fadiel, Wei Lu, et al.
The Journal of Infectious Diseases|June 16, 2007
Association of ICAM3 genetic variant with severe acute respiratory syndromeKelvin Y K Chan, Johannes C Y Ching, M S Xu, et al.
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