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Harinder Gill

Showing results (81-90 of 108) with videos related to

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Human Mutation|July 10, 2020
The expanding clinical phenotype of germline ABL1-associated congenital heart defects and skeletal malformations syndromeChun-An Chen, Emeline Crutcher, Harinder Gill, et al.
The American Journal of Gastroenterology|September 21, 2016
Association of Hepatitis B Core-Related Antigen With Hepatitis B Virus Reactivation in Occult Viral Carriers Undergoing High-Risk Immunosuppressive TherapyWai-Kay Seto, Danny Ka-Ho Wong, Thomas Sau-Yan Chan, et al.
Neuroscience|June 1, 2018
Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder PhenotypeGabriella A Horvath, Yulin Zhao, Maja Tarailo-Graovac, et al.
JCO Oncology Practice|July 17, 2025
Clinical Practice Recommendations for Myelofibrosis Management in the Asia-Pacific Region: The APAC-MF AllianceKeita Kirito, Chul Won Choi, Than Hein, et al.
Annals of Hematology|December 6, 2018
Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosisHarinder Gill, Ho-Wan Ip, Rita Yim, et al.
Cancer|March 27, 2018
Long-term outcome of relapsed acute promyelocytic leukemia treated with oral arsenic trioxide-based reinduction and maintenance regimens: A 15-year prospective studyHarinder Gill, Rita Yim, Harold K K Lee, et al.
Hepatology (Baltimore, Md.)|December 28, 2016
Hepatitis B reactivation in occult viral carriers undergoing hematopoietic stem cell transplantation: A prospective studyWai-Kay Seto, Thomas Sau-Yan Chan, Yu-Yan Hwang, et al.
BMC Pediatrics|January 21, 2021
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case reportGeraldine Blanchard-Rohner, Robert J Ragotte, Anne K Junker, et al.
Pediatric Neurology|April 16, 2025
Glycosylphosphatidylinositol Biosynthesis Defect Due To Novel Biallelic Pathogenic Variants in PIGWNazim Rabouhi, Smrithi Salian, Hind Benkerroum, et al.
American Journal of Human Genetics|December 26, 2017
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental DisordersVíctor Faundes, William G Newman, Laura Bernardini, et al.
Pageof 11

Showing results (81-90 of 108) with videos related to

Sort By:
Pageof 11
Human Mutation|July 10, 2020
The expanding clinical phenotype of germline ABL1-associated congenital heart defects and skeletal malformations syndromeChun-An Chen, Emeline Crutcher, Harinder Gill, et al.
The American Journal of Gastroenterology|September 21, 2016
Association of Hepatitis B Core-Related Antigen With Hepatitis B Virus Reactivation in Occult Viral Carriers Undergoing High-Risk Immunosuppressive TherapyWai-Kay Seto, Danny Ka-Ho Wong, Thomas Sau-Yan Chan, et al.
Neuroscience|June 1, 2018
Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder PhenotypeGabriella A Horvath, Yulin Zhao, Maja Tarailo-Graovac, et al.
JCO Oncology Practice|July 17, 2025
Clinical Practice Recommendations for Myelofibrosis Management in the Asia-Pacific Region: The APAC-MF AllianceKeita Kirito, Chul Won Choi, Than Hein, et al.
Annals of Hematology|December 6, 2018
Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosisHarinder Gill, Ho-Wan Ip, Rita Yim, et al.
Cancer|March 27, 2018
Long-term outcome of relapsed acute promyelocytic leukemia treated with oral arsenic trioxide-based reinduction and maintenance regimens: A 15-year prospective studyHarinder Gill, Rita Yim, Harold K K Lee, et al.
Hepatology (Baltimore, Md.)|December 28, 2016
Hepatitis B reactivation in occult viral carriers undergoing hematopoietic stem cell transplantation: A prospective studyWai-Kay Seto, Thomas Sau-Yan Chan, Yu-Yan Hwang, et al.
BMC Pediatrics|January 21, 2021
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case reportGeraldine Blanchard-Rohner, Robert J Ragotte, Anne K Junker, et al.
Pediatric Neurology|April 16, 2025
Glycosylphosphatidylinositol Biosynthesis Defect Due To Novel Biallelic Pathogenic Variants in PIGWNazim Rabouhi, Smrithi Salian, Hind Benkerroum, et al.
American Journal of Human Genetics|December 26, 2017
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental DisordersVíctor Faundes, William G Newman, Laura Bernardini, et al.
Pageof 11