Showing results (1-10 of 192) with videos related to
Sort By:
Pageof 20
Indian Journal of Pediatrics|June 10, 2003
Triple A syndrome--diagnostic and management issuesSunita Bijarnia, I C VermaIndian Journal of Pediatrics|March 29, 2003
Genetic counseling in acrocallosal syndromeSunita Bijarnia, Ashok Baijal, I C VermaIndian Pediatrics|August 18, 2014
Mitochondrial DNA depletion syndrome causing liver failureSunita Bijarnia-Mahay, Neelam Mohan, Deepak Goyal, et al.Indian Journal of Pediatrics|June 10, 2003
Genetic counseling and prenatal diagnosis in India--experience at Sir Ganga Ram HospitalI C Verma, Renu Saxena, Meena Lall, et al.Indian Pediatrics|January 16, 2021
Mutation and Phenotypic Spectrum of Patients With RASopathiesMeenakshi Lallar, Sunita Bijarnia-Mahay, I C Verma, et al.Indian Pediatrics|October 25, 2016
Ethylmalonic Encephalopathy in an Indian BoySunita Bijarnia-Mahay, Deepti Gupta, Yosuke Shigematsu, et al.Indian Journal of Pediatrics|June 11, 2014
Fanconi-Bickel syndrome - mutation in SLC2A2 geneMohit Kehar, Sunita Bijarnia, Sian Ellard, et al.Indian Pediatrics|October 23, 2019
Testing Modalities for Inborn Errors of Metabolism - What a Clinician Needs to Know?Sunita Bijarnia-Mahay, Seema KapoorIndian Journal of Pediatrics|April 2, 2010
Mutation studies in X-linked myotubular myopathy in three Indian familiesSunita Bijarnia, Ratna D Puri, Monika Jain, et al.JIMD Reports|May 13, 2020
Tyrosine hydroxylase deficiency-Clinical insights and a novel deletion in <i>TH</i> gene in an Indian patientSunita Bijarnia-Mahay, Vivek Jain, Beat ThönyPageof 20