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Wahab A Khan

Showing results (1-10 of 28) with videos related to

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Clinics in Laboratory Medicine|November 11, 2022
Utility of Fluorescence In Situ Hybridization in Clinical and Research ApplicationsGail H Vance, Wahab A Khan
Molecular Cytogenetics|December 19, 2014
Localized, non-random differences in chromatin accessibility between homologous metaphase chromosomesWahab A Khan, Peter K Rogan, Joan Hm Knoll
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|November 9, 2021
CRISPR-cas13 enzymology rapidly detects SARS-CoV-2 fragments in a clinical settingWahab A Khan, Rachael E Barney, Gregory J Tsongalis
Molecular Cytogenetics|August 10, 2011
Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 dupliconsWahab A Khan, Joan Hm Knoll, Peter K Rogan
Molecular Cytogenetics|August 15, 2015
Reversing chromatin accessibility differences that distinguish homologous mitotic metaphase chromosomesWahab A Khan, Peter K Rogan, Joan H M Knoll
BMC Medical Genomics|March 20, 2019
Familial inheritance of the 3q29 microdeletion syndrome: case report and reviewWahab A Khan, Ninette Cohen, Stuart A Scott, et al.
American Journal of Clinical Pathology|April 22, 2023
Validation of a rapid HLA-DQA1*05 pharmacogenomics assay to identify at-risk resistance to anti-tumor necrosis factor therapy among patients with inflammatory bowel diseaseRegina M DelBaugh, Leanne J Cook, Corey A Siegel, et al.
JAAD Case Reports|January 19, 2026
Novel isochromosome 7q and <i>NOTCH1</i> mutation in an 88-year-old male with Sézary syndromeNicole Loranger, Nicole Trepanowski, Jeremiah X Karrs, et al.
Brain Pathology (Zurich, Switzerland)|August 1, 2024
A pituitary mass in a 46-year-old womanFrancesco E Emiliani, Donald C Green, Edward G Hughes, et al.
American Journal of Medical Genetics. Part A|July 9, 2025
Novel Homozygous Full Gene Deletion of SLC12A5 in a Newborn With Refractory SeizuresLauren M Wainman, Dana L Wright, Nidhi D Shah, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Clinics in Laboratory Medicine|November 11, 2022
Utility of Fluorescence In Situ Hybridization in Clinical and Research ApplicationsGail H Vance, Wahab A Khan
Molecular Cytogenetics|December 19, 2014
Localized, non-random differences in chromatin accessibility between homologous metaphase chromosomesWahab A Khan, Peter K Rogan, Joan Hm Knoll
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|November 9, 2021
CRISPR-cas13 enzymology rapidly detects SARS-CoV-2 fragments in a clinical settingWahab A Khan, Rachael E Barney, Gregory J Tsongalis
Molecular Cytogenetics|August 10, 2011
Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 dupliconsWahab A Khan, Joan Hm Knoll, Peter K Rogan
Molecular Cytogenetics|August 15, 2015
Reversing chromatin accessibility differences that distinguish homologous mitotic metaphase chromosomesWahab A Khan, Peter K Rogan, Joan H M Knoll
BMC Medical Genomics|March 20, 2019
Familial inheritance of the 3q29 microdeletion syndrome: case report and reviewWahab A Khan, Ninette Cohen, Stuart A Scott, et al.
American Journal of Clinical Pathology|April 22, 2023
Validation of a rapid HLA-DQA1*05 pharmacogenomics assay to identify at-risk resistance to anti-tumor necrosis factor therapy among patients with inflammatory bowel diseaseRegina M DelBaugh, Leanne J Cook, Corey A Siegel, et al.
JAAD Case Reports|January 19, 2026
Novel isochromosome 7q and <i>NOTCH1</i> mutation in an 88-year-old male with Sézary syndromeNicole Loranger, Nicole Trepanowski, Jeremiah X Karrs, et al.
Brain Pathology (Zurich, Switzerland)|August 1, 2024
A pituitary mass in a 46-year-old womanFrancesco E Emiliani, Donald C Green, Edward G Hughes, et al.
American Journal of Medical Genetics. Part A|July 9, 2025
Novel Homozygous Full Gene Deletion of SLC12A5 in a Newborn With Refractory SeizuresLauren M Wainman, Dana L Wright, Nidhi D Shah, et al.
Pageof 3