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Plos One|February 8, 2014
Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong KongAnita S Y Kan, Elizabeth T Lau, W F Tang, et al.
European Journal of Medical Genetics|January 2, 2014
A prenatal case of split-hand malformation associated with 17p13.3 triplication - a dilemma in genetic counselingH M Luk, Vincent C H Wong, Ivan F M Lo, et al.
Scientific Reports|June 20, 2022
Germline variants of ATG7 in familial cholangiocarcinoma alter autophagy and p62Stephanie U Greer, Jiamin Chen, Margret H Ogmundsdottir, et al.
Plos One|October 22, 2014
The clinical impact of chromosomal microarray on paediatric care in Hong KongVictoria Q Tao, Kelvin Y K Chan, Yoyo W Y Chu, et al.
European Journal of Medical Genetics|April 12, 2014
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional careAnthony P Y Liu, Pak-Cheong Chow, Pamela P W Lee, et al.
NEJM AI|January 17, 2025
Prospective Multi-Site Validation of AI to Detect Tuberculosis and Chest X-Ray AbnormalitiesSahar Kazemzadeh, Atilla P Kiraly, Zaid Nabulsi, et al.
Plos Pathogens|April 19, 2019
Distinct phenotype and function of circulating Vδ1+ and Vδ2+ γδT-cells in acute and chronic hepatitis BKyong-Mi Chang, Daniel Traum, Jang-June Park, et al.
ACS Medicinal Chemistry Letters|October 24, 2017
Stabilizing a Tubulysin Antibody-Drug Conjugate To Enable Activity Against Multidrug-Resistant TumorsLeanna R Staben, Shang-Fan Yu, Jinhua Chen, et al.
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