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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 13, 2005
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Ching-Wan Lam, Yuet-Ping Yuen, Wai-Fun Cheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 5, 2019
Deoxythymidylate kinase, DTYMK, is a novel gene for mitochondrial DNA depletion syndrome
Ching-Wan Lam, Wai-Lan Yeung, Tsz-Ki Ling, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 21, 2010
Circulating fluorocytes at the first attack of acute intermittent porphyria: a missing link in the pathogenesis
Ching-Wan Lam, Kin-Chong Lau, Chloe Miu Mak, et al.
Blood Cells, Molecules & Diseases
|
December 10, 2014
Allogeneic haematopoietic stem cell transplantation for erythropoietic protoporphyria: a cautionary note
Carol Y M Cheung, Sidney Tam, Ching-Wan Lam, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2022
Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature
Hui-Yin Lo, Wai-Fu Ng, Nai-Chung Fong, et al.
The Lancet. Oncology
|
February 5, 2019
DPYD genotype-guided dose individualisation of fluoropyrimidine therapy: who and how?
Ka On Lam, Chi Chung Tong, Victor Ho Fun Lee, et al.
Chinese Medical Journal
|
February 28, 2004
Pearson's syndrome: a rare cause of non-immune hydrops fetalis
Chak Ho Li, Ching Wan Lam, Chi Wai Anselm Lee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 26, 2005
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormone
Ching-Wan Lam, Angel On-Kei Chan, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 16, 2006
Novel mutation, c.1234delA, in the DAX1 gene in congenital adrenal hypoplasia
Ching-Wan Lam, Anna Wai-Fun Cheng, Wing-Tat Poon, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 3, 2013
Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency
Sun Young Cho, Denise Li-Meng Goh, Kin-Chong Lau, et al.
Page
of 18
Search research articles
Search
Showing results (41-50 of 179) with videos related to
Sort By:
Page
of 18
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 13, 2005
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Ching-Wan Lam, Yuet-Ping Yuen, Wai-Fun Cheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 5, 2019
Deoxythymidylate kinase, DTYMK, is a novel gene for mitochondrial DNA depletion syndrome
Ching-Wan Lam, Wai-Lan Yeung, Tsz-Ki Ling, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 21, 2010
Circulating fluorocytes at the first attack of acute intermittent porphyria: a missing link in the pathogenesis
Ching-Wan Lam, Kin-Chong Lau, Chloe Miu Mak, et al.
Blood Cells, Molecules & Diseases
|
December 10, 2014
Allogeneic haematopoietic stem cell transplantation for erythropoietic protoporphyria: a cautionary note
Carol Y M Cheung, Sidney Tam, Ching-Wan Lam, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2022
Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature
Hui-Yin Lo, Wai-Fu Ng, Nai-Chung Fong, et al.
The Lancet. Oncology
|
February 5, 2019
DPYD genotype-guided dose individualisation of fluoropyrimidine therapy: who and how?
Ka On Lam, Chi Chung Tong, Victor Ho Fun Lee, et al.
Chinese Medical Journal
|
February 28, 2004
Pearson's syndrome: a rare cause of non-immune hydrops fetalis
Chak Ho Li, Ching Wan Lam, Chi Wai Anselm Lee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 26, 2005
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormone
Ching-Wan Lam, Angel On-Kei Chan, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 16, 2006
Novel mutation, c.1234delA, in the DAX1 gene in congenital adrenal hypoplasia
Ching-Wan Lam, Anna Wai-Fun Cheng, Wing-Tat Poon, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 3, 2013
Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency
Sun Young Cho, Denise Li-Meng Goh, Kin-Chong Lau, et al.
Page
of 18