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Inusha Panigrahi

Showing results (11-20 of 157) with videos related to

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Indian Journal of Human Genetics|September 30, 2011
Mutational spectrum of thalassemias in IndiaInusha Panigrahi, R K Marwaha
Journal of Pediatric Genetics|February 21, 2022
Over-Representation of Recessive Osteogenesis Imperfecta in Asian Indian ChildrenInusha Panigrahi, Yousaf Qureshi, Uwe Kornak
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Hypercortisolism and hypothyroidism in an infant with Smith-Lemli-Opitz syndromeSuresh Kumar, Renu Suthar, Inusha Panigrahi
American Journal of Medical Genetics. Part A|July 18, 2020
Indian child with novel variant in OFD1 geneInusha Panigrahi, Chirag Ahuja, Chakshu Chaudhry
Indian Pediatrics|May 28, 2003
Fowler-like syndrome with extreme oligohydramnios, growth restriction and without muscular hypoplasiaAshutosh Halder, Inusha Panigrahi, Lily Pal
BMJ Case Reports|June 22, 2011
Acquired syndactyly in epidermolysis bullosa dystrophicaInusha Panigrahi, Ketan Kulkarni, Devi Dayal
Prenatal Diagnosis|January 27, 2011
Non-invasive prenatal diagnosis: improved detection ratesInusha Panigrahi, Seema Thakur, Srinivasa Murthy
BMJ Case Reports|September 26, 2018
Novel mutation in the <i>CHST14</i> gene causing musculocontractural type of Ehlers-Danlos syndromeSapna Sandal, Anupriya Kaur, Inusha Panigrahi
Tropical Doctor|May 22, 2020
Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north IndiaDeepanjan Bhattacharya, Inusha Panigrahi, Chakshu Chaudhry
Journal of Pediatric Neurosciences|January 8, 2020
<i>KLHL40</i> Mutation Associated with Severe Nemaline Myopathy, Fetal Akinesia, and Cleft PalateKapil K Avasthi, Sarita Agarwal, Inusha Panigrahi
Pageof 16

Showing results (11-20 of 157) with videos related to

Sort By:
Pageof 16
Indian Journal of Human Genetics|September 30, 2011
Mutational spectrum of thalassemias in IndiaInusha Panigrahi, R K Marwaha
Journal of Pediatric Genetics|February 21, 2022
Over-Representation of Recessive Osteogenesis Imperfecta in Asian Indian ChildrenInusha Panigrahi, Yousaf Qureshi, Uwe Kornak
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Hypercortisolism and hypothyroidism in an infant with Smith-Lemli-Opitz syndromeSuresh Kumar, Renu Suthar, Inusha Panigrahi
American Journal of Medical Genetics. Part A|July 18, 2020
Indian child with novel variant in OFD1 geneInusha Panigrahi, Chirag Ahuja, Chakshu Chaudhry
Indian Pediatrics|May 28, 2003
Fowler-like syndrome with extreme oligohydramnios, growth restriction and without muscular hypoplasiaAshutosh Halder, Inusha Panigrahi, Lily Pal
BMJ Case Reports|June 22, 2011
Acquired syndactyly in epidermolysis bullosa dystrophicaInusha Panigrahi, Ketan Kulkarni, Devi Dayal
Prenatal Diagnosis|January 27, 2011
Non-invasive prenatal diagnosis: improved detection ratesInusha Panigrahi, Seema Thakur, Srinivasa Murthy
BMJ Case Reports|September 26, 2018
Novel mutation in the <i>CHST14</i> gene causing musculocontractural type of Ehlers-Danlos syndromeSapna Sandal, Anupriya Kaur, Inusha Panigrahi
Tropical Doctor|May 22, 2020
Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north IndiaDeepanjan Bhattacharya, Inusha Panigrahi, Chakshu Chaudhry
Journal of Pediatric Neurosciences|January 8, 2020
<i>KLHL40</i> Mutation Associated with Severe Nemaline Myopathy, Fetal Akinesia, and Cleft PalateKapil K Avasthi, Sarita Agarwal, Inusha Panigrahi
Pageof 16