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Lee-Jun Wong

Showing results (1-10 of 101) with videos related to

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Molecular Genetics and Metabolism|August 6, 2013
Diagnosis of mitochondrial myopathiesMargherita Milone, Lee-Jun Wong
Molecular Genetics and Metabolism Reports|November 30, 2016
Novel <i>OPA1</i> mutation featuring spastic paraparesis and intestinal dysmotilityMohamed Kazamel, Lee-Jun Wong, Margherita Milone
Neurology|November 16, 2011
POLG-related disorders: defects of the nuclear and mitochondrial genome interactionMargherita Milone, Eduardo E Benarroch, Lee-Jun Wong
Translational Research : the Journal of Laboratory and Clinical Medicine|July 26, 2018
Mitochondrial inheritance and cancerJing Dong, Lee-Jun Wong, Martha P Mims
Molecular Genetics and Metabolism Reports|July 18, 2018
Extra-muscular manifestations of TK2 deficiencyAyman W El-Hattab, Julia Wang, Lee-Jun Wong
Current Protocols in Human Genetics|January 15, 2011
Analysis of mitochondrial DNA point mutation heteroplasmy by ARMS quantitative PCRJing Wang, Victor Venegas, Fangyuan Li, et al.
Current Protocols in Human Genetics|January 15, 2011
Real-time quantitative PCR analysis of mitochondrial DNA contentVictor Venegas, Jing Wang, David Dimmock, et al.
Muscle & Nerve|February 12, 2009
Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutationOleg Shchelochkov, Lee-Jun Wong, Aziz Shaibani, et al.
Neuromuscular Disorders : NMD|May 23, 2015
Dystrophinopathy mimicking metabolic myopathiesTeerin Liewluck, Xia Tian, Lee-Jun Wong, et al.
The Journal of Molecular Diagnostics : JMD|June 17, 2008
Multiplex ligation-dependent probe amplification identification of whole exon and single nucleotide deletions in the CFTR gene of Hispanic individuals with cystic fibrosisIris Schrijver, Krista Rappahahn, Lynn Pique, et al.
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
Molecular Genetics and Metabolism|August 6, 2013
Diagnosis of mitochondrial myopathiesMargherita Milone, Lee-Jun Wong
Molecular Genetics and Metabolism Reports|November 30, 2016
Novel <i>OPA1</i> mutation featuring spastic paraparesis and intestinal dysmotilityMohamed Kazamel, Lee-Jun Wong, Margherita Milone
Neurology|November 16, 2011
POLG-related disorders: defects of the nuclear and mitochondrial genome interactionMargherita Milone, Eduardo E Benarroch, Lee-Jun Wong
Translational Research : the Journal of Laboratory and Clinical Medicine|July 26, 2018
Mitochondrial inheritance and cancerJing Dong, Lee-Jun Wong, Martha P Mims
Molecular Genetics and Metabolism Reports|July 18, 2018
Extra-muscular manifestations of TK2 deficiencyAyman W El-Hattab, Julia Wang, Lee-Jun Wong
Current Protocols in Human Genetics|January 15, 2011
Analysis of mitochondrial DNA point mutation heteroplasmy by ARMS quantitative PCRJing Wang, Victor Venegas, Fangyuan Li, et al.
Current Protocols in Human Genetics|January 15, 2011
Real-time quantitative PCR analysis of mitochondrial DNA contentVictor Venegas, Jing Wang, David Dimmock, et al.
Muscle & Nerve|February 12, 2009
Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutationOleg Shchelochkov, Lee-Jun Wong, Aziz Shaibani, et al.
Neuromuscular Disorders : NMD|May 23, 2015
Dystrophinopathy mimicking metabolic myopathiesTeerin Liewluck, Xia Tian, Lee-Jun Wong, et al.
The Journal of Molecular Diagnostics : JMD|June 17, 2008
Multiplex ligation-dependent probe amplification identification of whole exon and single nucleotide deletions in the CFTR gene of Hispanic individuals with cystic fibrosisIris Schrijver, Krista Rappahahn, Lynn Pique, et al.
Pageof 11