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The Indian Journal of Medical Research|June 23, 2017
Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in IndiaSudhisha Dubey, Veronique Tardy, Madhumita Roy Chowdhury, et al.Molecular Syndromology|January 29, 2021
Eyes See what the Mind Knows: Clues to Pattern Recognition in Single Enzyme Deficiency-Related Peroxisomal DisordersVeronica Arora, Sunita Bijarnia-Mahay, Sudhisha Dubey, et al.Molecular Diagnosis & Therapy|April 9, 2009
Study of NAT2 gene polymorphisms in an Indian population: association with plasma isoniazid concentration in a cohort of tuberculosis patientsNeera Singh, Sudhisha Dubey, Saravanan Chinnaraj, et al.JIMD Reports|March 13, 2015
Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian PatientsNeerja Gupta, Pawan Kumar Singh, Manoj Kumar, et al.Fertility and Sterility|October 15, 2003
Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disordersRavinder Goswami, Deepti Goswami, Madhulika Kabra, et al.Fetal and Pediatric Pathology|September 8, 2011
Limb/pelvis-hypoplasia/aplasia syndrome--further delineation of phenotypeNeerja Gupta, Madhulika KabraIndian Journal of Pediatrics|June 18, 2011
Acute management of sick infants with suspected inborn errors of metabolismNeerja Gupta, Madhulika KabraCurrent Microbiology|April 2, 2004
Mercury volatilization by R factor systems in Escherichia coli isolated from aquatic environments of IndiaNeerja Gupta, Arif AliIndian Pediatrics|May 31, 2007
Recent advances in approach to treatment of genetic disorders: clinicians perspectiveNeerja Gupta, Madhulika KabraPageof 20