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Inusha Panigrahi

Showing results (81-90 of 158) with videos related to

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Indian Pediatrics|September 18, 2014
Thyroid dysfunction in Indian children with Down syndromeDevi Dayal, Puneet Jain, Inusha Panigrahi, et al.
Journal of Pediatric Genetics|November 6, 2024
<i>TWIST1</i> Gene Variants Cause Craniosynostosis with Limb Abnormalities in Asian PatientsShalini Dhiman, Inusha Panigrahi, Maryada Sharma, et al.
Journal of Pediatric Genetics|May 9, 2024
Case Studies of Two Classical Imprinting Growth Disorders: Silver-Russell and Beckwith-Wiedemann SyndromesParminder Kaur, Chakshu Chaudhry, Anupriya Kaur, et al.
Annals of Hematology|June 3, 2009
A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfacesRavindra Kumar, Parag M Tamhankar, Inusha Panigrahi, et al.
Case Reports in Genetics|September 12, 2024
Intellectual Disability and Blended Phenotypes: Insights from a Centre in North IndiaInusha Panigrahi, Sudha Rao, Shalu Verma Kumar, et al.
Indian Journal of Pediatrics|December 17, 2009
Seckel syndrome with chromosomal 18 deletionInusha Panigrahi, Satvinder Kaur, Ketan Kulkarni, et al.
American Journal of Medical Genetics. Part A|June 17, 2026
Novel Homozygous Exonic Deletion of the TMEM17 Gene Associated With Meckel-Gruber Syndrome PhenotypeInusha Panigrahi, Sneha Sagarkar, Udhaya Kotecha, et al.
Pediatric Blood & Cancer|July 15, 2011
Xmn1-G γ polymorphism and clinical predictors of severity of disease in β-thalassemia intermediaSapna Oberoi, Reena Das, Inusha Panigrahi, et al.
Indian Pediatrics|September 13, 2024
Auxological Dynamics of Cephalic Index in Indian Children with Down Syndrome: A Longitudinal StudyHarvinder Kaur, Anil Kumar Bhalla, Rupinder Kaur, et al.
Indian Journal of Human Genetics|September 11, 2013
Proteus syndrome: Clinical profile of six patients and review of literatureSuresh Kumar Angurana, Renu Suthar Angurana, Inusha Panigrahi, et al.
Pageof 16

Showing results (81-90 of 158) with videos related to

Sort By:
Pageof 16
Indian Pediatrics|September 18, 2014
Thyroid dysfunction in Indian children with Down syndromeDevi Dayal, Puneet Jain, Inusha Panigrahi, et al.
Journal of Pediatric Genetics|November 6, 2024
<i>TWIST1</i> Gene Variants Cause Craniosynostosis with Limb Abnormalities in Asian PatientsShalini Dhiman, Inusha Panigrahi, Maryada Sharma, et al.
Journal of Pediatric Genetics|May 9, 2024
Case Studies of Two Classical Imprinting Growth Disorders: Silver-Russell and Beckwith-Wiedemann SyndromesParminder Kaur, Chakshu Chaudhry, Anupriya Kaur, et al.
Annals of Hematology|June 3, 2009
A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfacesRavindra Kumar, Parag M Tamhankar, Inusha Panigrahi, et al.
Case Reports in Genetics|September 12, 2024
Intellectual Disability and Blended Phenotypes: Insights from a Centre in North IndiaInusha Panigrahi, Sudha Rao, Shalu Verma Kumar, et al.
Indian Journal of Pediatrics|December 17, 2009
Seckel syndrome with chromosomal 18 deletionInusha Panigrahi, Satvinder Kaur, Ketan Kulkarni, et al.
American Journal of Medical Genetics. Part A|June 17, 2026
Novel Homozygous Exonic Deletion of the TMEM17 Gene Associated With Meckel-Gruber Syndrome PhenotypeInusha Panigrahi, Sneha Sagarkar, Udhaya Kotecha, et al.
Pediatric Blood & Cancer|July 15, 2011
Xmn1-G γ polymorphism and clinical predictors of severity of disease in β-thalassemia intermediaSapna Oberoi, Reena Das, Inusha Panigrahi, et al.
Indian Pediatrics|September 13, 2024
Auxological Dynamics of Cephalic Index in Indian Children with Down Syndrome: A Longitudinal StudyHarvinder Kaur, Anil Kumar Bhalla, Rupinder Kaur, et al.
Indian Journal of Human Genetics|September 11, 2013
Proteus syndrome: Clinical profile of six patients and review of literatureSuresh Kumar Angurana, Renu Suthar Angurana, Inusha Panigrahi, et al.
Pageof 16