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Thorax
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April 24, 2009
The PHF11 gene is not associated with asthma or asthma phenotypes in two independent populations
J McClenaghan, N M Warrington, E F Jamrozik, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
December 7, 2016
A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients
C Y Law, W L Yeung, Y F Cheung, et al.
The American Journal of Gastroenterology
|
March 24, 2007
Detection of hypermethylated DNA or cyclooxygenase-2 messenger RNA in fecal samples of patients with colorectal cancer or polyps
Wai K Leung, Ka-Fai To, Ellen P S Man, et al.
Plos Genetics
|
October 5, 2021
Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation
Silke Fuchs, William T Garrood, Anna Beber, et al.
The American Journal of Gastroenterology
|
September 27, 2005
Quantitative detection of promoter hypermethylation in multiple genes in the serum of patients with colorectal cancer
Wai K Leung, Ka-Fai To, Ellen P S Man, et al.
BMC Medical Ethics
|
November 2, 2022
The view of Hong Kong parents on secondary use of dried blood spots in newborn screening program
L L Hui, E A S Nelson, H B Deng, et al.
Journal of Gastroenterology and Hepatology
|
August 18, 2020
Short Message Service reminders reduce outpatient colonoscopy nonattendance rate: A randomized controlled study
Thomas Y T Lam, Aric J Hui, Felix Sia, et al.
Allergy
|
March 3, 2016
Identification of STOML2 as a putative novel asthma risk gene associated with IL6R
J A Revez, M C Matheson, J Hui, et al.
The American Journal of Gastroenterology
|
June 27, 2007
Initial treatment with lansoprazole in young dyspeptic patients with negative urea breath test result: a randomized controlled trial with 12-month follow-up
Wai K Leung, Justin C Y Wu, Francis K L Chan, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
Primary plasmalemmal carnitine transporter defect manifested with dicarboxylic aciduria and impaired fatty acid oxidation
N L Tang, J Hui, L K Law, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 192) with videos related to
Sort By:
Page
of 20
Thorax
|
April 24, 2009
The PHF11 gene is not associated with asthma or asthma phenotypes in two independent populations
J McClenaghan, N M Warrington, E F Jamrozik, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
December 7, 2016
A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients
C Y Law, W L Yeung, Y F Cheung, et al.
The American Journal of Gastroenterology
|
March 24, 2007
Detection of hypermethylated DNA or cyclooxygenase-2 messenger RNA in fecal samples of patients with colorectal cancer or polyps
Wai K Leung, Ka-Fai To, Ellen P S Man, et al.
Plos Genetics
|
October 5, 2021
Resistance to a CRISPR-based gene drive at an evolutionarily conserved site is revealed by mimicking genotype fixation
Silke Fuchs, William T Garrood, Anna Beber, et al.
The American Journal of Gastroenterology
|
September 27, 2005
Quantitative detection of promoter hypermethylation in multiple genes in the serum of patients with colorectal cancer
Wai K Leung, Ka-Fai To, Ellen P S Man, et al.
BMC Medical Ethics
|
November 2, 2022
The view of Hong Kong parents on secondary use of dried blood spots in newborn screening program
L L Hui, E A S Nelson, H B Deng, et al.
Journal of Gastroenterology and Hepatology
|
August 18, 2020
Short Message Service reminders reduce outpatient colonoscopy nonattendance rate: A randomized controlled study
Thomas Y T Lam, Aric J Hui, Felix Sia, et al.
Allergy
|
March 3, 2016
Identification of STOML2 as a putative novel asthma risk gene associated with IL6R
J A Revez, M C Matheson, J Hui, et al.
The American Journal of Gastroenterology
|
June 27, 2007
Initial treatment with lansoprazole in young dyspeptic patients with negative urea breath test result: a randomized controlled trial with 12-month follow-up
Wai K Leung, Justin C Y Wu, Francis K L Chan, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
Primary plasmalemmal carnitine transporter defect manifested with dicarboxylic aciduria and impaired fatty acid oxidation
N L Tang, J Hui, L K Law, et al.
Page
of 20