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Inusha Panigrahi

Showing results (31-40 of 158) with videos related to

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Journal of Genetics|July 9, 2021
Single gene variants causing deafness in Asian IndiansInusha Panigrahi, Divya Kumari, B N Anil Kumar
Pediatrics and Neonatology|January 31, 2024
Non-immune hydrops fetalis due to infantile sialidosisInusha Panigrahi, Sudhanshu Grover, Mahesh Hiranandani, et al.
American Journal of Medical Genetics. Part A|September 11, 2020
Wolf-Hirschhorn syndrome: A case series from IndiaChakshu Chaudhry, Anit Kaur, Inusha Panigrahi, et al.
Indian Journal of Pediatrics|June 30, 2011
Sickle cell anemia--molecular diagnosis and prenatal counseling: SGPGI experienceRavindra Kumar, Inusha Panigrahi, Ashwin Dalal, et al.
Mediterranean Journal of Hematology and Infectious Diseases|January 26, 2013
Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and DiagnosisRavindra Kumar, Kritanjali Singh, Inusha Panigrahi, et al.
BMJ Case Reports|July 4, 2012
Hemifacial microsomia with pulmonary hypoplasiaInusha Panigrahi, Rashmi Ranjan Das, Ram Kumar Marwaha
Neonatology|February 16, 2008
Urinary malondialdehyde levels in newborns following delivery room resuscitationAshok Kumar, Inusha Panigrahi, Sriparna Basu, et al.
Current Pediatric Reviews|March 16, 2022
Clinical and Molecular Heterogeneity of Silver-Russell Syndrome and Therapeutic Challenges: A Systematic ReviewAmit Singh, Ketan Pajni, Inusha Panigrahi, et al.
Molecular Genetics and Genomics : MGG|September 2, 2015
Primordial dwarfism: overview of clinical and genetic aspectsPreeti Khetarpal, Satrupa Das, Inusha Panigrahi, et al.
Current Pediatric Reviews|April 9, 2024
Novel Compound Heterozygous Mutations of LIG4 Gene in an Indian LIG4 Syndrome Patient with Severe Microcephaly: Case Report, In-silico Analysis and Systematic ReviewAmit Singh, Sabyasachi Senapati, Inusha Panigrahi, et al.
Pageof 16

Showing results (31-40 of 158) with videos related to

Sort By:
Pageof 16
Journal of Genetics|July 9, 2021
Single gene variants causing deafness in Asian IndiansInusha Panigrahi, Divya Kumari, B N Anil Kumar
Pediatrics and Neonatology|January 31, 2024
Non-immune hydrops fetalis due to infantile sialidosisInusha Panigrahi, Sudhanshu Grover, Mahesh Hiranandani, et al.
American Journal of Medical Genetics. Part A|September 11, 2020
Wolf-Hirschhorn syndrome: A case series from IndiaChakshu Chaudhry, Anit Kaur, Inusha Panigrahi, et al.
Indian Journal of Pediatrics|June 30, 2011
Sickle cell anemia--molecular diagnosis and prenatal counseling: SGPGI experienceRavindra Kumar, Inusha Panigrahi, Ashwin Dalal, et al.
Mediterranean Journal of Hematology and Infectious Diseases|January 26, 2013
Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and DiagnosisRavindra Kumar, Kritanjali Singh, Inusha Panigrahi, et al.
BMJ Case Reports|July 4, 2012
Hemifacial microsomia with pulmonary hypoplasiaInusha Panigrahi, Rashmi Ranjan Das, Ram Kumar Marwaha
Neonatology|February 16, 2008
Urinary malondialdehyde levels in newborns following delivery room resuscitationAshok Kumar, Inusha Panigrahi, Sriparna Basu, et al.
Current Pediatric Reviews|March 16, 2022
Clinical and Molecular Heterogeneity of Silver-Russell Syndrome and Therapeutic Challenges: A Systematic ReviewAmit Singh, Ketan Pajni, Inusha Panigrahi, et al.
Molecular Genetics and Genomics : MGG|September 2, 2015
Primordial dwarfism: overview of clinical and genetic aspectsPreeti Khetarpal, Satrupa Das, Inusha Panigrahi, et al.
Current Pediatric Reviews|April 9, 2024
Novel Compound Heterozygous Mutations of LIG4 Gene in an Indian LIG4 Syndrome Patient with Severe Microcephaly: Case Report, In-silico Analysis and Systematic ReviewAmit Singh, Sabyasachi Senapati, Inusha Panigrahi, et al.
Pageof 16