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Neerja Gupta

Showing results (151-160 of 238) with videos related to

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Cytogenetic and Genome Research|September 10, 2015
Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in IndiaPankaj Sharma, Neerja Gupta, Madhumita R Chowdhury, et al.
Prenatal Diagnosis|July 24, 2021
Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisAlec Reginald Errol Correa, Kamal Naini, Pallavi Mishra, et al.
Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.
Journal of Clinical Neuromuscular Disease|February 26, 2019
Thenar Hypertrophy and Electrical Myotonia in Pompe DiseasePrashant Jauhari, Arushi Gahlot Saini, Renu Suthar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 6, 2011
Molecular analysis of ABCD1 gene in Indian patients with X-linked adrenoleukodystrophyPallavi Shukla, Neerja Gupta, Sheffali Gulati, et al.
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.
Pediatric Neurology|January 3, 2021
Association of Sleep Apnea With Development and Behavior in Down Syndrome: A Prospective Clinical and Polysomnographic StudyVaishakh Anand, Garima Shukla, Neerja Gupta, et al.
Indian Journal of Pediatrics|July 14, 2012
Prevalence of celiac disease in Indian children with Down syndrome and its clinical and laboratory predictorsAbdus Sami Bhat, Mona K Chaturvedi, Savita Saini, et al.
BMC Medical Genetics|October 28, 2019
Decoding of novel missense TSC2 gene variants using in-silico methodsShruthi Sudarshan, Manoj Kumar, Punit Kaur, et al.
Clinical Dysmorphology|April 20, 2016
Pycnodysostosis: mutation spectrum in five unrelated Indian childrenKausik Mandal, Sayantan Ray, Deepti Saxena, et al.
Pageof 24

Showing results (151-160 of 238) with videos related to

Sort By:
Pageof 24
Cytogenetic and Genome Research|September 10, 2015
Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in IndiaPankaj Sharma, Neerja Gupta, Madhumita R Chowdhury, et al.
Prenatal Diagnosis|July 24, 2021
Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisAlec Reginald Errol Correa, Kamal Naini, Pallavi Mishra, et al.
Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.
Journal of Clinical Neuromuscular Disease|February 26, 2019
Thenar Hypertrophy and Electrical Myotonia in Pompe DiseasePrashant Jauhari, Arushi Gahlot Saini, Renu Suthar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 6, 2011
Molecular analysis of ABCD1 gene in Indian patients with X-linked adrenoleukodystrophyPallavi Shukla, Neerja Gupta, Sheffali Gulati, et al.
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.
Pediatric Neurology|January 3, 2021
Association of Sleep Apnea With Development and Behavior in Down Syndrome: A Prospective Clinical and Polysomnographic StudyVaishakh Anand, Garima Shukla, Neerja Gupta, et al.
Indian Journal of Pediatrics|July 14, 2012
Prevalence of celiac disease in Indian children with Down syndrome and its clinical and laboratory predictorsAbdus Sami Bhat, Mona K Chaturvedi, Savita Saini, et al.
BMC Medical Genetics|October 28, 2019
Decoding of novel missense TSC2 gene variants using in-silico methodsShruthi Sudarshan, Manoj Kumar, Punit Kaur, et al.
Clinical Dysmorphology|April 20, 2016
Pycnodysostosis: mutation spectrum in five unrelated Indian childrenKausik Mandal, Sayantan Ray, Deepti Saxena, et al.
Pageof 24