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Annual Review of Analytical Chemistry (Palo Alto, Calif.)|February 23, 2026
The Next Generation of Protein Sequencing and Analysis MethodsKingsley L-J Wong, Mattias Tolhurst, Oren A Fox, et al.European Journal of Pediatrics|July 1, 1997
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapyC W Lam, C H Lau, J C Williams, et al.Molecular Genetics and Metabolism|August 28, 1998
3849 + 10 kb C --> T splicing mutation in Hispanic CF patientsM H Liang, K K Wertz, C M Bowman, et al.Neuropediatrics|November 11, 2008
Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRIN Brunetti-Pierri, K Selby, M O'Sullivan, et al.Molecular Genetics and Metabolism|June 30, 2000
A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II geneG D Vladutiu, M J Bennett, D Smail, et al.Clinical Molecular Pathology|October 1, 1995
Diagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes in a Chinese family by PCR/restriction enzyme analysisC W Lam, K Jain, K Y Chan, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 8, 2001
Hereditary nonpolyposis colorectal cancer with gynecologic malignancies: report of two families in TaiwanC H Chen, R L Huang, M S Yu, et al.Journal of Paediatrics and Child Health|February 13, 2001
De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspringC H Ko, C W Lam, P W Tse, et al.Advanced Materials (Deerfield Beach, Fla.)|September 6, 2025
Mixed Ionic and Electronic Charge Transport in Conductive Protein Fibers Revealed with DC Electrical MeasurementsDaniel Modafferi, Xinxin Hao, Kingsley L-J Wong, et al.Human Mutation|October 23, 2001
Improved detection of CFTR mutations in Southern California Hispanic CF patientsL J Wong, J Wang, Y H Zhang, et al.Pageof 7