Search research articles
Contact Us
Filters
Showing results (31-40 of 179) with videos related to
Page
of 18
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 6, 2013
Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient
Sun Young Cho, Tak-Shing Siu, Oliver Ma, et al.
Journal of Human Genetics
|
February 2, 2021
Postzygotic inactivating mutation of KIF13A located at chromosome 6p22.3 in a patient with a novel mosaic neuroectodermal syndrome
Ching-Wan Lam, Candace Yim Chan, Ka-Chung Wong, et al.
Molecular Genetics and Metabolism
|
February 22, 2002
Novel donor splice site mutation of ABCG5 gene in sitosterolemia
Ching-Wan Lam, Anna Wai-Fun Cheng, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 4, 2008
DNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese population
Kin-Chong Lau, Ching-Wan Lam, Bonnie Fong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 2, 2008
Rapid diagnosis of Wilson disease by a 28-mutation panel: real-time amplification refractory mutation system in diagnosing acute Wilsonian liver failure
Chloe M Mak, Ching-Wan Lam, Sik-To Lai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 10, 2014
Quantitative metabolomics of urine for rapid etiological diagnosis of urinary tract infection: evaluation of a microbial-mammalian co-metabolite as a diagnostic biomarker
Ching-Wan Lam, Chun-Yiu Law, Kong-Hung Sze, et al.
Brain & Development
|
December 27, 2005
Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease
Wai Lan Yeung, Ching Wan Lam, Joannie Hui, et al.
Critical Reviews in Clinical Laboratory Sciences
|
December 4, 2013
Inborn errors of metabolism and expanded newborn screening: review and update
Chloe Miu Mak, Han-Chih Hencher Lee, Albert Yan-Wo Chan, et al.
Cureus
|
December 9, 2025
Slow-Channel Congenital Myasthenic Syndrome due to a CHRNA1 Variant Masquerading as Atypical Anorexia Nervosa: A Case Report
Timothy Ming Him Yeung, Yuan Gao, Chun Fung So, et al.
Clinical Biochemistry
|
October 1, 2025
Pregnancy or PEG? Polyethylene glycol causes false positive pregnancy test
Timothy Ming Him Yeung, Elaine Yi Ling Wong, Melody Yee Man Wong, et al.
Page
of 18
Search research articles
Search
Showing results (31-40 of 179) with videos related to
Sort By:
Page
of 18
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 6, 2013
Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient
Sun Young Cho, Tak-Shing Siu, Oliver Ma, et al.
Journal of Human Genetics
|
February 2, 2021
Postzygotic inactivating mutation of KIF13A located at chromosome 6p22.3 in a patient with a novel mosaic neuroectodermal syndrome
Ching-Wan Lam, Candace Yim Chan, Ka-Chung Wong, et al.
Molecular Genetics and Metabolism
|
February 22, 2002
Novel donor splice site mutation of ABCG5 gene in sitosterolemia
Ching-Wan Lam, Anna Wai-Fun Cheng, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 4, 2008
DNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese population
Kin-Chong Lau, Ching-Wan Lam, Bonnie Fong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 2, 2008
Rapid diagnosis of Wilson disease by a 28-mutation panel: real-time amplification refractory mutation system in diagnosing acute Wilsonian liver failure
Chloe M Mak, Ching-Wan Lam, Sik-To Lai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 10, 2014
Quantitative metabolomics of urine for rapid etiological diagnosis of urinary tract infection: evaluation of a microbial-mammalian co-metabolite as a diagnostic biomarker
Ching-Wan Lam, Chun-Yiu Law, Kong-Hung Sze, et al.
Brain & Development
|
December 27, 2005
Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease
Wai Lan Yeung, Ching Wan Lam, Joannie Hui, et al.
Critical Reviews in Clinical Laboratory Sciences
|
December 4, 2013
Inborn errors of metabolism and expanded newborn screening: review and update
Chloe Miu Mak, Han-Chih Hencher Lee, Albert Yan-Wo Chan, et al.
Cureus
|
December 9, 2025
Slow-Channel Congenital Myasthenic Syndrome due to a CHRNA1 Variant Masquerading as Atypical Anorexia Nervosa: A Case Report
Timothy Ming Him Yeung, Yuan Gao, Chun Fung So, et al.
Clinical Biochemistry
|
October 1, 2025
Pregnancy or PEG? Polyethylene glycol causes false positive pregnancy test
Timothy Ming Him Yeung, Elaine Yi Ling Wong, Melody Yee Man Wong, et al.
Page
of 18