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

Kabra

Showing results (721-730 of 1,518) with videos related to

Pageof 152
Sort By:
Reproductive Biomedicine Online|August 22, 2003
Nucleolar precursor body distribution in pronuclei is correlated to chromosomal abnormalities in embryosSerdar Coskun, Ali Hellani, Kamal Jaroudi, et al.
Indian Journal of Pediatrics|March 7, 2003
Etiology of acute lower respiratory tract infectionS K Kabra, Rakesh Lodha, S Broor, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenarioManjula Maheshwari, R Vijaya, Manju Ghosh, et al.
Indian Journal of Pediatrics|August 10, 2000
Biotinidase deficiency--a treatable entityS Gulati, G R Passi, A Kumar, et al.
Journal of Child Neurology|April 9, 2013
Dystrophinopathy diagnosis made easy: skin biopsy, an emerging novel toolBiswaroop Chakrabarty, M C Sharma, Sheffali Gulati, et al.
The National Medical Journal of India|December 5, 2014
Thoracic neuroblastoma presenting as recurrent empyemaRashmi Ranjan Das, Abdus Sami, Rachna Seth, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|October 8, 2020
Functional Outcomes at 1 Year After PICU Discharge in Critically Ill Children With Severe SepsisJhuma Sankar, Sravanthi Moodu, Kiran Kumar, et al.
Journal of Child Neurology|February 15, 2017
Validation of Polymerase Chain Reaction-Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome PatientsMadhumita Roy Chowdhury, Sandeepa Chauhan, Anjali Dabral, et al.
Indian Journal of Pediatrics|April 1, 2008
Approach to inborn errors of metabolism presenting in the neonateSuvasini Sharma, Pradeep Kumar, Ramesh Agarwal, et al.
Journal of Pediatric Neurosciences|June 4, 2014
Menkes disease - An important cause of early onset refractory seizuresPuneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, et al.
Pageof 152

Showing results (721-730 of 1,518) with videos related to

Sort By:
Pageof 152
Reproductive Biomedicine Online|August 22, 2003
Nucleolar precursor body distribution in pronuclei is correlated to chromosomal abnormalities in embryosSerdar Coskun, Ali Hellani, Kamal Jaroudi, et al.
Indian Journal of Pediatrics|March 7, 2003
Etiology of acute lower respiratory tract infectionS K Kabra, Rakesh Lodha, S Broor, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenarioManjula Maheshwari, R Vijaya, Manju Ghosh, et al.
Indian Journal of Pediatrics|August 10, 2000
Biotinidase deficiency--a treatable entityS Gulati, G R Passi, A Kumar, et al.
Journal of Child Neurology|April 9, 2013
Dystrophinopathy diagnosis made easy: skin biopsy, an emerging novel toolBiswaroop Chakrabarty, M C Sharma, Sheffali Gulati, et al.
The National Medical Journal of India|December 5, 2014
Thoracic neuroblastoma presenting as recurrent empyemaRashmi Ranjan Das, Abdus Sami, Rachna Seth, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|October 8, 2020
Functional Outcomes at 1 Year After PICU Discharge in Critically Ill Children With Severe SepsisJhuma Sankar, Sravanthi Moodu, Kiran Kumar, et al.
Journal of Child Neurology|February 15, 2017
Validation of Polymerase Chain Reaction-Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome PatientsMadhumita Roy Chowdhury, Sandeepa Chauhan, Anjali Dabral, et al.
Indian Journal of Pediatrics|April 1, 2008
Approach to inborn errors of metabolism presenting in the neonateSuvasini Sharma, Pradeep Kumar, Ramesh Agarwal, et al.
Journal of Pediatric Neurosciences|June 4, 2014
Menkes disease - An important cause of early onset refractory seizuresPuneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, et al.
Pageof 152