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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 21, 2015
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsyChun-Yiu Law, Sharon Tzu-Lun Chang, Sun Young Cho, et al.
Human Mutation|August 31, 2002
Genotype-phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemiaLisa Y S Chan, Ching-Wan Lam, Ying-Tat Mak, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 25, 2014
Dystroglycanopathy with two novel POMT1 mutations in a Chinese boy with developmental delay and muscular dystrophyYeow Kuan Chong, Louis Che Kwan Ma, Kit Lin Lo, et al.
Current Problems in Cardiology|May 12, 2024
Multi-year population-based analysis of Asian patients with acute decompensated heart failure and advanced chronic kidney diseaseSamuel S Tan, Wenchy Yy Tan, Lucy S Zheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 2015
Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and strokeChing-Wan Lam, Chun-Yiu Law, Wai-Kwan Siu, et al.
Leukemia Research|May 27, 2006
Solid tumors subsequent to arsenic trioxide treatment for acute promyelocytic leukemiaWing-Yan Au, Cyrus R Kumana, Ching-Wan Lam, et al.
Experimental Biology and Medicine (Maywood, N.J.)|April 25, 2015
Laboratory diagnosis of melioidosis: past, present and futureSusanna K P Lau, Siddharth Sridhar, Chi-Chun Ho, et al.
Cancer Genetics and Cytogenetics|December 31, 2002
Cryptic t(X;18), ins(6;18), and SYT-SSX2 gene fusion in a case of intraneural monophasic synovial sarcomaValia S Lestou, John X O'Connell, Marc Robichaud, et al.
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