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Malika Seth

Showing results (1-10 of 6) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 27, 2006
Cognitive enhancement with central thalamic electrical stimulationPrasad Shirvalkar, Malika Seth, Nicholas D Schiff, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 17, 2021
Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel <i>LOXL3</i> MutationAnubhuti Sood, Uzma Shamim, Om P Kharbanda, et al.
Human Mutation|September 9, 2020
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in IndiaAnkita Narang, Bharathram Uppilli, Asokachandran Vivekanand, et al.
Neurogenetics|August 1, 2021
A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patientsKiran Polavarapu, Aradhna Mathur, Aditi Joshi, et al.
Neurobiology of Aging|February 10, 2020
C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilectionUzma Shamim, Sakshi Ambawat, Jyotsna Singh, et al.
Advanced Genetics (Hoboken, N.J.)|January 9, 2023
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening ToolPooja Sharma, Akhilesh Kumar Sonakar, Nishu Tyagi, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2006
Cognitive enhancement with central thalamic electrical stimulationPrasad Shirvalkar, Malika Seth, Nicholas D Schiff, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 17, 2021
Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel <i>LOXL3</i> MutationAnubhuti Sood, Uzma Shamim, Om P Kharbanda, et al.
Human Mutation|September 9, 2020
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in IndiaAnkita Narang, Bharathram Uppilli, Asokachandran Vivekanand, et al.
Neurogenetics|August 1, 2021
A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patientsKiran Polavarapu, Aradhna Mathur, Aditi Joshi, et al.
Neurobiology of Aging|February 10, 2020
C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilectionUzma Shamim, Sakshi Ambawat, Jyotsna Singh, et al.
Advanced Genetics (Hoboken, N.J.)|January 9, 2023
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening ToolPooja Sharma, Akhilesh Kumar Sonakar, Nishu Tyagi, et al.
Pageof 1