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Inusha Panigrahi

Showing results (111-120 of 159) with videos related to

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Gene|October 22, 2017
CRELD1 gene variants and atrioventricular septal defects in Down syndromeAmbreen Asim, Sarita Agarwal, Inusha Panigrahi, et al.
Neurology India|May 9, 2006
Role of MTHFR C677T polymorphism in ischemic strokeInusha Panigrahi, Tathagata Chatterjee, Arijit Biswas, et al.
European Journal of Medical Genetics|February 27, 2018
Novel mutation in a family with WNT1-related osteoporosisInusha Panigrahi, Siyaram Didel, Harita Kirpal, et al.
Haematologica|September 8, 2006
Molecular characterization of thalassemia intermedia in IndiansInusha Panigrahi, Sarita Agarwal, Mandakini Pradhan, et al.
Neurology India|September 21, 2018
Identification of microdeletion and microduplication syndromes by chromosomal microarray in patients with intellectual disability with dysmorphismInusha Panigrahi, Puneet Jain, Siyaram Didel, et al.
Scientific Reports|November 27, 2022
Development of a new screening method for faster kinship analyses in mass disasters: a proof of concept studySonia Kakkar, Phulen Sarma, Inusha Panigrahi, et al.
JAMA Dermatology|May 1, 2018
Warty Fingers and Toes in a Child With Congenital Lymphedema: Elephantiasis Nostras VerrucosaAnuradha Bishnoi, Keshavamurthy Vinay, Vikarn Vishwajeet, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|November 16, 2020
Ten-year use of recombinant parathyroid hormone for the treatment of hypoparathyroidism in a boy with partial Jacobsen syndromeDevi Dayal, Inusha Panigrahi, Tandra Varma, et al.
Laboratory Medicine|January 29, 2021
Achondroplasia-First Report from India of a Rare FGFR3 Gene VariantChakshu Chaudhry, Prabakaran G, Priyanka Srivastava, et al.
Indian Journal of Pathology & Microbiology|August 29, 2006
Therapy-related acute promyelocytic leukemia after treatment of carcinoma breast--a case reportMaitreyee Bhattacharyya, Tathagata Chatterjee, Inusha Panigrahi, et al.
Pageof 16

Showing results (111-120 of 159) with videos related to

Sort By:
Pageof 16
Gene|October 22, 2017
CRELD1 gene variants and atrioventricular septal defects in Down syndromeAmbreen Asim, Sarita Agarwal, Inusha Panigrahi, et al.
Neurology India|May 9, 2006
Role of MTHFR C677T polymorphism in ischemic strokeInusha Panigrahi, Tathagata Chatterjee, Arijit Biswas, et al.
European Journal of Medical Genetics|February 27, 2018
Novel mutation in a family with WNT1-related osteoporosisInusha Panigrahi, Siyaram Didel, Harita Kirpal, et al.
Haematologica|September 8, 2006
Molecular characterization of thalassemia intermedia in IndiansInusha Panigrahi, Sarita Agarwal, Mandakini Pradhan, et al.
Neurology India|September 21, 2018
Identification of microdeletion and microduplication syndromes by chromosomal microarray in patients with intellectual disability with dysmorphismInusha Panigrahi, Puneet Jain, Siyaram Didel, et al.
Scientific Reports|November 27, 2022
Development of a new screening method for faster kinship analyses in mass disasters: a proof of concept studySonia Kakkar, Phulen Sarma, Inusha Panigrahi, et al.
JAMA Dermatology|May 1, 2018
Warty Fingers and Toes in a Child With Congenital Lymphedema: Elephantiasis Nostras VerrucosaAnuradha Bishnoi, Keshavamurthy Vinay, Vikarn Vishwajeet, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|November 16, 2020
Ten-year use of recombinant parathyroid hormone for the treatment of hypoparathyroidism in a boy with partial Jacobsen syndromeDevi Dayal, Inusha Panigrahi, Tandra Varma, et al.
Laboratory Medicine|January 29, 2021
Achondroplasia-First Report from India of a Rare FGFR3 Gene VariantChakshu Chaudhry, Prabakaran G, Priyanka Srivastava, et al.
Indian Journal of Pathology & Microbiology|August 29, 2006
Therapy-related acute promyelocytic leukemia after treatment of carcinoma breast--a case reportMaitreyee Bhattacharyya, Tathagata Chatterjee, Inusha Panigrahi, et al.
Pageof 16