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Inusha Panigrahi

Showing results (41-50 of 158) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|October 23, 2009
Zolendronate in osteogenesis imperfectaInusha Panigrahi, Rashmi Ranjan Das, Ram Kumar Marwaha
Clinical Dysmorphology|October 29, 2002
Mental retardation, ptosis and polydactyly: a new autosomal recessive syndrome?Inusha Panigrahi, Shubha R Phadke, S S Agarwal
Annals of Hematology|August 6, 2009
Long-term response to deferiprone therapy in Asian IndiansInusha Panigrahi, Ram K Marwaha, Rashmi R Das
Molecular Biology Reports|May 18, 2011
STR markers for detecting heterogeneity in Indian populationShalu Jain, Inusha Panigrahi, Jayesh Sheth, et al.
Pediatric Neurology|March 25, 2015
Seizure as the presenting manifestation in Griscelli syndrome type 2Inusha Panigrahi, Renu Suthar, Amit Rawat, et al.
Journal of Pediatric Genetics|January 1, 2024
Chromosome 1p36 Deletion Syndrome: Four Patients with Variable PresentationsChakshu Chaudhry, Divya Kumari, Inusha Panigrahi, et al.
Journal of Pediatric Genetics|January 23, 2023
Genetic Defects in Children with Cardiac Anomalies/Malformations: Noonan and CFC SyndromesDivya Kumari, Deepti Chaudhary, Inusha Panigrahi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|July 16, 2021
Study of Prothrombotic Gene Variations Associated with the Risk of Development of Thrombosis in Patients with Down SyndromeChandreswara Raju Kataru, Vinodhini Krishnakumar, Inusha Panigrahi, et al.
Indian Journal of Human Genetics|November 20, 2012
Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literatureSuresh Kumar, Renu Suthar, Inusha Panigrahi, et al.
BMJ Case Reports|April 22, 2019
Hunter syndrome with persistent thrombocytopeniaInusha Panigrahi, Manoj Dhanorkar, Siyaram Didel, et al.
Pageof 16

Showing results (41-50 of 158) with videos related to

Sort By:
Pageof 16
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 23, 2009
Zolendronate in osteogenesis imperfectaInusha Panigrahi, Rashmi Ranjan Das, Ram Kumar Marwaha
Clinical Dysmorphology|October 29, 2002
Mental retardation, ptosis and polydactyly: a new autosomal recessive syndrome?Inusha Panigrahi, Shubha R Phadke, S S Agarwal
Annals of Hematology|August 6, 2009
Long-term response to deferiprone therapy in Asian IndiansInusha Panigrahi, Ram K Marwaha, Rashmi R Das
Molecular Biology Reports|May 18, 2011
STR markers for detecting heterogeneity in Indian populationShalu Jain, Inusha Panigrahi, Jayesh Sheth, et al.
Pediatric Neurology|March 25, 2015
Seizure as the presenting manifestation in Griscelli syndrome type 2Inusha Panigrahi, Renu Suthar, Amit Rawat, et al.
Journal of Pediatric Genetics|January 1, 2024
Chromosome 1p36 Deletion Syndrome: Four Patients with Variable PresentationsChakshu Chaudhry, Divya Kumari, Inusha Panigrahi, et al.
Journal of Pediatric Genetics|January 23, 2023
Genetic Defects in Children with Cardiac Anomalies/Malformations: Noonan and CFC SyndromesDivya Kumari, Deepti Chaudhary, Inusha Panigrahi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|July 16, 2021
Study of Prothrombotic Gene Variations Associated with the Risk of Development of Thrombosis in Patients with Down SyndromeChandreswara Raju Kataru, Vinodhini Krishnakumar, Inusha Panigrahi, et al.
Indian Journal of Human Genetics|November 20, 2012
Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literatureSuresh Kumar, Renu Suthar, Inusha Panigrahi, et al.
BMJ Case Reports|April 22, 2019
Hunter syndrome with persistent thrombocytopeniaInusha Panigrahi, Manoj Dhanorkar, Siyaram Didel, et al.
Pageof 16