Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sameer Bhatia

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Indian Journal of Pediatrics|June 15, 2026
Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic DisordersAnju Shukla, Sameer Bhatia, Mounika Endrakanti, et al.
Indian Pediatrics|April 22, 2021
Challenges in Chronic Genetic Disorders: Lessons From the COVID-19 PandemicSwasti Pal, Sameer Bhatia, Sunita Bijarnia-Mahay, et al.
Medical Journal, Armed Forces India|July 14, 2016
Bochdalek Hernia in A ChildA K Dubey, Kirandeep Sodhi, Arvind Gupta, et al.
Indian Journal of Pediatrics|March 5, 2024
CEDNIK Syndrome - A Report of a Clinically Recognizable Disorder with Prenatal DiagnosisSunita Bijarnia-Mahay, Sameer Bhatia, Deepti Gupta, et al.
Industrial Psychiatry Journal|February 20, 2018
Cross-sectional study of anxiety symptoms in students in preexamination periodPrateek Yadav, Vinay Singh Chauhan, P S Bhat, et al.
European Journal of Medical Genetics|August 18, 2023
A report of 5 Indian families with multicentric carpotarsal osteolysis syndromeNeerja Gupta, Soumalya Chakraborty, Madhumita Roy Chowdhury, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Role of next generation sequencing in diagnosis and management of critically ill children with suspected monogenic disorderSameer Bhatia, Swasti Pal, Samarth Kulshrestha, et al.
Journal of Cellular and Molecular Medicine|March 7, 2026
Bioengineered AAV9 and Optimised Microdystrophin Vectors Augment Phenotypic Rescue in a Murine Model of Duchenne Muscular DystrophyMohankumar B Senthilkumar, Sanya Sharma, Navaneeth Srinivasan, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Indian Journal of Pediatrics|June 15, 2026
Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic DisordersAnju Shukla, Sameer Bhatia, Mounika Endrakanti, et al.
Indian Pediatrics|April 22, 2021
Challenges in Chronic Genetic Disorders: Lessons From the COVID-19 PandemicSwasti Pal, Sameer Bhatia, Sunita Bijarnia-Mahay, et al.
Medical Journal, Armed Forces India|July 14, 2016
Bochdalek Hernia in A ChildA K Dubey, Kirandeep Sodhi, Arvind Gupta, et al.
Indian Journal of Pediatrics|March 5, 2024
CEDNIK Syndrome - A Report of a Clinically Recognizable Disorder with Prenatal DiagnosisSunita Bijarnia-Mahay, Sameer Bhatia, Deepti Gupta, et al.
Industrial Psychiatry Journal|February 20, 2018
Cross-sectional study of anxiety symptoms in students in preexamination periodPrateek Yadav, Vinay Singh Chauhan, P S Bhat, et al.
European Journal of Medical Genetics|August 18, 2023
A report of 5 Indian families with multicentric carpotarsal osteolysis syndromeNeerja Gupta, Soumalya Chakraborty, Madhumita Roy Chowdhury, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Role of next generation sequencing in diagnosis and management of critically ill children with suspected monogenic disorderSameer Bhatia, Swasti Pal, Samarth Kulshrestha, et al.
Journal of Cellular and Molecular Medicine|March 7, 2026
Bioengineered AAV9 and Optimised Microdystrophin Vectors Augment Phenotypic Rescue in a Murine Model of Duchenne Muscular DystrophyMohankumar B Senthilkumar, Sanya Sharma, Navaneeth Srinivasan, et al.
Pageof 2