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Priyanshu Mathur

Showing results (1-10 of 6) with videos related to

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Indian Pediatrics|April 29, 2026
GeneticsPriyanshu Mathur
Case Reports in Pediatrics|December 23, 2016
Fetal Valproate Syndrome with Limb Defects: An Indian Case ReportManisha Goyal, Ashok Gupta, Manish Sharma, et al.
Global Medical Genetics|February 10, 2025
Limb-Girdle Muscular Dystrophies (LGMD): Clinical features, diagnosis and genetic variability through next generation sequencingPriyanshu Mathur, Ashmeet Kaur, Urvashi Vijay, et al.
Global Medical Genetics|March 3, 2025
Unlocking the genetic blueprint of duchenne muscular dystrophy: A personalized approach with MLPA and WESPriyanshu Mathur, Ashmeet Kaur, Kamlesh Kumar Agarwal, et al.
Indian Journal of Otolaryngology and Head and Neck Surgery : Official Publication of the Association of Otolaryngologists of India|November 17, 2023
A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing ImpairmentAakanksha Dadhich, Shruti Bhargava, Sunil Samdhani, et al.
Indian Journal of Pediatrics|March 8, 2022
Antiviral Therapy in Cytomegalovirus-Associated Biliary AtresiaPraveen Mathur, Priyanka Udawat, Priyanshu Mathur, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Indian Pediatrics|April 29, 2026
GeneticsPriyanshu Mathur
Case Reports in Pediatrics|December 23, 2016
Fetal Valproate Syndrome with Limb Defects: An Indian Case ReportManisha Goyal, Ashok Gupta, Manish Sharma, et al.
Global Medical Genetics|February 10, 2025
Limb-Girdle Muscular Dystrophies (LGMD): Clinical features, diagnosis and genetic variability through next generation sequencingPriyanshu Mathur, Ashmeet Kaur, Urvashi Vijay, et al.
Global Medical Genetics|March 3, 2025
Unlocking the genetic blueprint of duchenne muscular dystrophy: A personalized approach with MLPA and WESPriyanshu Mathur, Ashmeet Kaur, Kamlesh Kumar Agarwal, et al.
Indian Journal of Otolaryngology and Head and Neck Surgery : Official Publication of the Association of Otolaryngologists of India|November 17, 2023
A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing ImpairmentAakanksha Dadhich, Shruti Bhargava, Sunil Samdhani, et al.
Indian Journal of Pediatrics|March 8, 2022
Antiviral Therapy in Cytomegalovirus-Associated Biliary AtresiaPraveen Mathur, Priyanka Udawat, Priyanshu Mathur, et al.
Pageof 1