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Shing H Zhan

Showing results (11-20 of 17) with videos related to

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Biorxiv : the Preprint Server for Biology|November 26, 2025
A Pandemic-Scale Ancestral Recombination Graph for SARS-CoV-2Shing H Zhan, Yan Wong, Anastasia Ignatieva, et al.
Scientific Reports|January 31, 2024
Mass spectrometry in IgG4-related disease diagnosisDaniel C Onwuka, Luke Y C Chen, Shing H Zhan, et al.
The Canadian Journal of Cardiology|January 28, 2014
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defectSteven C Greenway, Ross McLeod, Stacey Hume, et al.
American Journal of Human Genetics|May 15, 2012
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeDan Doherty, Albert E Chudley, Gail Coghlan, et al.
Acta Neuropathologica|November 28, 2012
Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastomaAdrian M Dubuc, Marc Remke, Andrey Korshunov, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
American Journal of Human Genetics|October 22, 2013
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humansJan Halbritter, Albane A Bizet, Miriam Schmidts, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Biorxiv : the Preprint Server for Biology|November 26, 2025
A Pandemic-Scale Ancestral Recombination Graph for SARS-CoV-2Shing H Zhan, Yan Wong, Anastasia Ignatieva, et al.
Scientific Reports|January 31, 2024
Mass spectrometry in IgG4-related disease diagnosisDaniel C Onwuka, Luke Y C Chen, Shing H Zhan, et al.
The Canadian Journal of Cardiology|January 28, 2014
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defectSteven C Greenway, Ross McLeod, Stacey Hume, et al.
American Journal of Human Genetics|May 15, 2012
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeDan Doherty, Albert E Chudley, Gail Coghlan, et al.
Acta Neuropathologica|November 28, 2012
Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastomaAdrian M Dubuc, Marc Remke, Andrey Korshunov, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
American Journal of Human Genetics|October 22, 2013
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humansJan Halbritter, Albane A Bizet, Miriam Schmidts, et al.
Pageof 2