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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.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.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.European Journal of Radiology|January 26, 2022
Post-mortem MRI in stillbirth: Normal imaging appearancesNeerja Gupta, Amit Gupta, Atin Kumar, et al.Journal of Pediatric Genetics|September 15, 2016
Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12pPankaj Sharma, Neerja Gupta, Madhumita R Chowdhury, et al.The Indian Journal of Radiology & Imaging|March 19, 2021
Spine radiograph in dysplasias: A pictorial essayPavan Gabra, Manisha Jana, Priyanka Naranje, et al.Practical Neurology|July 8, 2022
Late-onset cobalamin C disease: rare but treatableAminu Aliyar, Mounika Endrakanti, Rajesh K Singh, et al.Pageof 21