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

J Patil

Showing results (371-380 of 377) with videos related to

Pageof 38
Sort By:
You have reached the last page of results.This site can display upto 377 results.
American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.
Clinical Genetics|July 24, 2021
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalitiesParneet Kaur, Michelle C do Rosario, Malavika Hebbar, et al.
European Journal of Human Genetics : EJHG|December 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Purvi Majethia, Karthik Nair, et al.
Clinical Genetics|February 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implicationsPurvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
American Journal of Human Genetics|December 12, 2018
Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial DysmorphismJoshi Stephen, Sateesh Maddirevula, Sheela Nampoothiri, et al.
American Journal of Medical Genetics. Part A|July 28, 2017
Noonan syndrome in diverse populationsPaul Kruszka, Antonio R Porras, Yonit A Addissie, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Williams-Beuren syndrome in diverse populationsPaul Kruszka, Antonio R Porras, Deise Helena de Souza, et al.
Pageof 38

Showing results (371-380 of 377) with videos related to

Sort By:
Pageof 38
You have reached the last page of results.This site can display upto 377 results.
American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.
Clinical Genetics|July 24, 2021
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalitiesParneet Kaur, Michelle C do Rosario, Malavika Hebbar, et al.
European Journal of Human Genetics : EJHG|December 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Purvi Majethia, Karthik Nair, et al.
Clinical Genetics|February 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implicationsPurvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
American Journal of Human Genetics|December 12, 2018
Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial DysmorphismJoshi Stephen, Sateesh Maddirevula, Sheela Nampoothiri, et al.
American Journal of Medical Genetics. Part A|July 28, 2017
Noonan syndrome in diverse populationsPaul Kruszka, Antonio R Porras, Yonit A Addissie, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Williams-Beuren syndrome in diverse populationsPaul Kruszka, Antonio R Porras, Deise Helena de Souza, et al.
Pageof 38