Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ching-Wan Lam

Showing results (81-90 of 179) with videos related to

Pageof 18
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 24, 2006
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1bChing-Wan Lam, Matthew Shu-Ching Yan, Tat-Yin Law, et al.
Lancet (London, England)|August 25, 2009
Mutational analysis for Wilson's diseaseWai Kay Seto, Chloe Miu Mak, David But, et al.
Chinese Medical Journal|August 2, 2003
Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected deathChing-Wan Lam, Chi-Kong Lai, Chun-Bong Chow, et al.
Journal of Human Genetics|October 13, 2006
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinityChing-Wan Lam, Sui-Fan Tong, Keong Wong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 8, 2014
NMR-based urinalysis for beta-ketothiolase deficiencyChun-Yiu Law, Ching-Wan Lam, Chor-kwan Ching, et al.
Frontiers in Medicine|March 14, 2022
An Unsupervised Machine Learning Clustering and Prediction of Differential Clinical Phenotypes of COVID-19 Patients Based on Blood Tests-A Hong Kong Population StudyKitty Yu-Yeung Lau, Kei-Shing Ng, Ka-Wai Kwok, et al.
Chinese Medical Journal|December 18, 2004
A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VIChing-wan Lam, Angel On-kei Chan, Chi-kong Lai, et al.
Pathology|March 26, 2011
Application of pharmacogenetics: UGT1A1*28 and nilotinib-induced unconjugated hyperbilirubinaemia in a patient with chronic myeloid leukaemiaSammy Pak-lam Chen, Wing-tat Poon, Chloe Miu Mak, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|August 9, 2003
[Mutation-function analysis in the lipoprotein lipase gene of Chinese patients with hypertriglyceridemic type 2 diabetes]Tao Yang, Ching-wan Lam, Man-wo Tsang, et al.
International Journal of Cancer|March 18, 2004
RASSF1A is a target tumor suppressor from 3p21.3 in nasopharyngeal carcinomaLillian Shuk-Nga Chow, Kwok-Wai Lo, Joseph Kwong, et al.
Pageof 18

Showing results (81-90 of 179) with videos related to

Sort By:
Pageof 18
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 24, 2006
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1bChing-Wan Lam, Matthew Shu-Ching Yan, Tat-Yin Law, et al.
Lancet (London, England)|August 25, 2009
Mutational analysis for Wilson's diseaseWai Kay Seto, Chloe Miu Mak, David But, et al.
Chinese Medical Journal|August 2, 2003
Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected deathChing-Wan Lam, Chi-Kong Lai, Chun-Bong Chow, et al.
Journal of Human Genetics|October 13, 2006
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinityChing-Wan Lam, Sui-Fan Tong, Keong Wong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 8, 2014
NMR-based urinalysis for beta-ketothiolase deficiencyChun-Yiu Law, Ching-Wan Lam, Chor-kwan Ching, et al.
Frontiers in Medicine|March 14, 2022
An Unsupervised Machine Learning Clustering and Prediction of Differential Clinical Phenotypes of COVID-19 Patients Based on Blood Tests-A Hong Kong Population StudyKitty Yu-Yeung Lau, Kei-Shing Ng, Ka-Wai Kwok, et al.
Chinese Medical Journal|December 18, 2004
A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VIChing-wan Lam, Angel On-kei Chan, Chi-kong Lai, et al.
Pathology|March 26, 2011
Application of pharmacogenetics: UGT1A1*28 and nilotinib-induced unconjugated hyperbilirubinaemia in a patient with chronic myeloid leukaemiaSammy Pak-lam Chen, Wing-tat Poon, Chloe Miu Mak, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|August 9, 2003
[Mutation-function analysis in the lipoprotein lipase gene of Chinese patients with hypertriglyceridemic type 2 diabetes]Tao Yang, Ching-wan Lam, Man-wo Tsang, et al.
International Journal of Cancer|March 18, 2004
RASSF1A is a target tumor suppressor from 3p21.3 in nasopharyngeal carcinomaLillian Shuk-Nga Chow, Kwok-Wai Lo, Joseph Kwong, et al.
Pageof 18