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Neerja Gupta

Showing results (101-110 of 237) with videos related to

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Indian Pediatrics|February 16, 2020
Mevalonate Kinase Deficiency as Cause of Periodic Fever in Two SiblingsAlec Reginald Errol Correa, Neerja Gupta, Narendra Bagri, et al.
Indian Journal of Pediatrics|May 1, 2016
Spondylometaphyseal Dysplasia Corner Fracture (Sutcliffe) TypeNikhil Nair, Amit Kumar Satapathy, Neerja Gupta, et al.
American Journal of Medical Genetics. Part A|January 6, 2022
Monosomy 1p36: Report of a cohort of 13 Asian Indian patientsNeerja Gupta, Ravneet Kaur, Shubha Phadke, et al.
The Indian Journal of Medical Research|September 1, 2018
Spectrum of <i>GJB2</i> gene variants in Indian children with non-syndromic hearing lossPawan Kumar Singh, Shipra Sharma, Manju Ghosh, et al.
American Journal of Medical Genetics. Part A|March 8, 2026
High Metabolic Syndrome Prevalence in Down Syndrome Children: Need for New GuidelinesSelvamanojkumar Sundaravel, Neerja Gupta, Vandana Jain, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 1, 2024
Personalized management of hepatic glycogen storage disorders: The role of continuous glucose monitoringAmbika Gupta, Anuja Agarwala, Mani Kalaivani, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian originRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Clinical Dysmorphology|September 8, 2006
A female with hemihypertrophy and chylous ascites - Klippel-Trenaunay syndrome or Proteus syndrome: a diagnostic dilemmaNeerja Gupta, Madhulika Kabra, Konanki Ramesh, et al.
Pageof 24

Showing results (101-110 of 237) with videos related to

Sort By:
Pageof 24
Indian Pediatrics|February 16, 2020
Mevalonate Kinase Deficiency as Cause of Periodic Fever in Two SiblingsAlec Reginald Errol Correa, Neerja Gupta, Narendra Bagri, et al.
Indian Journal of Pediatrics|May 1, 2016
Spondylometaphyseal Dysplasia Corner Fracture (Sutcliffe) TypeNikhil Nair, Amit Kumar Satapathy, Neerja Gupta, et al.
American Journal of Medical Genetics. Part A|January 6, 2022
Monosomy 1p36: Report of a cohort of 13 Asian Indian patientsNeerja Gupta, Ravneet Kaur, Shubha Phadke, et al.
The Indian Journal of Medical Research|September 1, 2018
Spectrum of <i>GJB2</i> gene variants in Indian children with non-syndromic hearing lossPawan Kumar Singh, Shipra Sharma, Manju Ghosh, et al.
American Journal of Medical Genetics. Part A|March 8, 2026
High Metabolic Syndrome Prevalence in Down Syndrome Children: Need for New GuidelinesSelvamanojkumar Sundaravel, Neerja Gupta, Vandana Jain, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 1, 2024
Personalized management of hepatic glycogen storage disorders: The role of continuous glucose monitoringAmbika Gupta, Anuja Agarwala, Mani Kalaivani, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian originRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Clinical Dysmorphology|September 8, 2006
A female with hemihypertrophy and chylous ascites - Klippel-Trenaunay syndrome or Proteus syndrome: a diagnostic dilemmaNeerja Gupta, Madhulika Kabra, Konanki Ramesh, et al.
Pageof 24