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

Neerja Gupta

Showing results (71-80 of 237) with videos related to

Pageof 24
Sort By:
Indian Pediatrics|May 10, 2016
Ghosal Type Hematodiaphyseal DysplasiaAmrit Jeevan, Mathilde Doyard, Madhulika Kabra, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Distinct de novo deletions in a brother-sister pair with RTT: a case reportKirti Mittal, Neerja Gupta, Madhulika Kabra, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 2, 2008
Carbimazole embryopathy-bilateral choanal atresia and patent vitello-intestinal duct: a case report and review of literatureLakshminarayanan Kannan, Satish Mishra, Ramesh Agarwal, et al.
Annals of Human Genetics|March 3, 2021
Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrumAlec Reginald Errol Correa, Mounika Endrakanti, Kamal Naini, et al.
Indian Journal of Pediatrics|August 7, 2012
Imaging in neonatal maple syrup urine diseasePuneet Jain, Suvasini Sharma, Naveen Sankhyan, et al.
American Journal of Medical Genetics. Part A|November 20, 2021
First case report of Penttinen syndrome from IndiaBhawana Aggarwal, Alec R E Correa, Neerja Gupta, et al.
Journal of Pediatric Genetics|August 14, 2019
Report of Two Novel Mutations in Indian Patients with Rothmund-Thomson SyndromeSakshi Yadav, Seema Thakur, Juergen Kohlhase, et al.
Annals of Indian Academy of Neurology|August 30, 2016
The spectrum of leukodystrophies in children: Experience at a tertiary care centre from North IndiaSheffali Gulati, Puneet Jain, Biswaroop Chakrabarty, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 11, 2012
Schwartz Jampel syndrome in childrenRavindra Arya, Suvasini Sharma, Neerja Gupta, et al.
American Journal of Medical Genetics. Part A|May 21, 2020
Bi-allelic loss-of-function novel variants in LTBP3-related skeletal dysplasia: Report of first patient from IndiaRavneet Kaur, Ishrat Siddiqui, Vijay Mathur, et al.
Pageof 24

Showing results (71-80 of 237) with videos related to

Sort By:
Pageof 24
Indian Pediatrics|May 10, 2016
Ghosal Type Hematodiaphyseal DysplasiaAmrit Jeevan, Mathilde Doyard, Madhulika Kabra, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Distinct de novo deletions in a brother-sister pair with RTT: a case reportKirti Mittal, Neerja Gupta, Madhulika Kabra, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 2, 2008
Carbimazole embryopathy-bilateral choanal atresia and patent vitello-intestinal duct: a case report and review of literatureLakshminarayanan Kannan, Satish Mishra, Ramesh Agarwal, et al.
Annals of Human Genetics|March 3, 2021
Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrumAlec Reginald Errol Correa, Mounika Endrakanti, Kamal Naini, et al.
Indian Journal of Pediatrics|August 7, 2012
Imaging in neonatal maple syrup urine diseasePuneet Jain, Suvasini Sharma, Naveen Sankhyan, et al.
American Journal of Medical Genetics. Part A|November 20, 2021
First case report of Penttinen syndrome from IndiaBhawana Aggarwal, Alec R E Correa, Neerja Gupta, et al.
Journal of Pediatric Genetics|August 14, 2019
Report of Two Novel Mutations in Indian Patients with Rothmund-Thomson SyndromeSakshi Yadav, Seema Thakur, Juergen Kohlhase, et al.
Annals of Indian Academy of Neurology|August 30, 2016
The spectrum of leukodystrophies in children: Experience at a tertiary care centre from North IndiaSheffali Gulati, Puneet Jain, Biswaroop Chakrabarty, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 11, 2012
Schwartz Jampel syndrome in childrenRavindra Arya, Suvasini Sharma, Neerja Gupta, et al.
American Journal of Medical Genetics. Part A|May 21, 2020
Bi-allelic loss-of-function novel variants in LTBP3-related skeletal dysplasia: Report of first patient from IndiaRavneet Kaur, Ishrat Siddiqui, Vijay Mathur, et al.
Pageof 24