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HGG Advances
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February 8, 2025
Multifaceted analysis of noncoding and coding de novo variants implicates NOTCH signaling pathway in tetralogy of Fallot in Chinese population
Qiongfen Lin, Detao Zhang, Peter J Gruber, et al.
Plos One
|
July 11, 2013
Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia
Long Cui, Emily Hoi-Man Wong, Guo Cheng, et al.
Journal of the Peripheral Nervous System : JPNS
|
April 2, 2009
-459C>T point mutation in 5' non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathy
Miaoxin Li, Tat-Sun Cheng, Philip W-L Ho, et al.
Nucleic Acids Research
|
November 29, 2015
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
Mulin Jun Li, Zipeng Liu, Panwen Wang, et al.
Emerging Microbes & Infections
|
June 4, 2015
Identification and characterization of a novel incompatibility group X3 plasmid carrying bla NDM-1 in Enterobacteriaceae isolates with epidemiological links to multiple geographical areas in China
Pak-Leung Ho, Zhen Li, Wai-U Lo, et al.
Thrombosis and Haemostasis
|
February 6, 2010
A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men
Kwok Leung Ong, Annette W K Tso, Stacey S Cherny, et al.
Psychological Medicine
|
October 9, 2020
Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study
Gloria Hoi-Yee Li, Ching-Lung Cheung, Albert Kar-Kin Chung, et al.
American Journal of Hypertension
|
August 12, 2011
Relationship of plasma interleukin-6 and its genetic variants with hypertension in Hong Kong Chinese
Bernard M Y Cheung, Kwok Leung Ong, Annette W K Tso, et al.
Annals of Human Genetics
|
April 16, 2024
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele
Larry Baum, Chi Chiu Lee, Rui Ye, et al.
Bioinformatics (Oxford, England)
|
June 9, 2016
Predicting regulatory variants with composite statistic
Mulin Jun Li, Zhicheng Pan, Zipeng Liu, et al.
Page
of 23
Search research articles
Search
Showing results (101-110 of 224) with videos related to
Sort By:
Page
of 23
HGG Advances
|
February 8, 2025
Multifaceted analysis of noncoding and coding de novo variants implicates NOTCH signaling pathway in tetralogy of Fallot in Chinese population
Qiongfen Lin, Detao Zhang, Peter J Gruber, et al.
Plos One
|
July 11, 2013
Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia
Long Cui, Emily Hoi-Man Wong, Guo Cheng, et al.
Journal of the Peripheral Nervous System : JPNS
|
April 2, 2009
-459C>T point mutation in 5' non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathy
Miaoxin Li, Tat-Sun Cheng, Philip W-L Ho, et al.
Nucleic Acids Research
|
November 29, 2015
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
Mulin Jun Li, Zipeng Liu, Panwen Wang, et al.
Emerging Microbes & Infections
|
June 4, 2015
Identification and characterization of a novel incompatibility group X3 plasmid carrying bla NDM-1 in Enterobacteriaceae isolates with epidemiological links to multiple geographical areas in China
Pak-Leung Ho, Zhen Li, Wai-U Lo, et al.
Thrombosis and Haemostasis
|
February 6, 2010
A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men
Kwok Leung Ong, Annette W K Tso, Stacey S Cherny, et al.
Psychological Medicine
|
October 9, 2020
Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study
Gloria Hoi-Yee Li, Ching-Lung Cheung, Albert Kar-Kin Chung, et al.
American Journal of Hypertension
|
August 12, 2011
Relationship of plasma interleukin-6 and its genetic variants with hypertension in Hong Kong Chinese
Bernard M Y Cheung, Kwok Leung Ong, Annette W K Tso, et al.
Annals of Human Genetics
|
April 16, 2024
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele
Larry Baum, Chi Chiu Lee, Rui Ye, et al.
Bioinformatics (Oxford, England)
|
June 9, 2016
Predicting regulatory variants with composite statistic
Mulin Jun Li, Zhicheng Pan, Zipeng Liu, et al.
Page
of 23