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Gautham Arunachal

Showing results (1-10 of 121) with videos related to

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Indian Journal of Pediatrics|August 31, 2019
Van der Woude Syndrome: IRF6 MutationsAnsa P Sunny, Gautham Arunachal, Sumita Danda
Current Opinion in Psychiatry|March 28, 2012
Epidemiology of comorbid substance use and psychiatric disorders in AsiaJagadisha Thirthalli, Channaveerachari Naveen Kumar, Gautham Arunachal
Parkinsonism & Related Disorders|September 28, 2025
SPTBN2- associated early-onset Parkinson's disease: A phenotypic expansionRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Parkinsonism & Related Disorders|October 9, 2024
Adult-onset cranio-cervical segmental dystonia due to ADAR1 gene mutation: A novel phenotypeRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Clinical Dysmorphology|April 5, 2016
A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring-Opitz syndromeGautham Arunachal, Sumita Danda, Sabita Omprakash, et al.
European Journal of Medical Genetics|August 3, 2018
A family with floppy neonates with severe respiratory insufficiency: A lethal phenotype of RFT1-CDG due to a novel mutationThangaraj Abiramalatha, Gautham Arunachal, Karthik Muthusamy, et al.
Indian Journal of Pediatrics|June 15, 2019
Genomics and Radiogenomics in Inherited Neurometabolic Disorders - A Practical Primer for PediatriciansSniya Valsa Sudhakar, Karthik Muthusamy, Gautham Arunachal, et al.
Indian Journal of Psychiatry|February 13, 2019
Clinical Practice Guidelines for Assessment and Management of intellectual disabilityM Thomas Kishore, Gautham Arunachal Udipi, Shekhar P Seshadri
Scientific Reports|May 24, 2017
Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohortNikhat Khan, Anuja Lipsa, Gautham Arunachal, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|October 25, 2024
Adult-Onset EIF2B-Pathies: A Clinical, Imaging and Genetic Profiling with Literature ReviewSangeeth Thuppanattumadam Ananthasubramanian, Gautham Arunachal, Hansashree Padmanabha, et al.
Pageof 13

Showing results (1-10 of 121) with videos related to

Sort By:
Pageof 13
Indian Journal of Pediatrics|August 31, 2019
Van der Woude Syndrome: IRF6 MutationsAnsa P Sunny, Gautham Arunachal, Sumita Danda
Current Opinion in Psychiatry|March 28, 2012
Epidemiology of comorbid substance use and psychiatric disorders in AsiaJagadisha Thirthalli, Channaveerachari Naveen Kumar, Gautham Arunachal
Parkinsonism & Related Disorders|September 28, 2025
SPTBN2- associated early-onset Parkinson's disease: A phenotypic expansionRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Parkinsonism & Related Disorders|October 9, 2024
Adult-onset cranio-cervical segmental dystonia due to ADAR1 gene mutation: A novel phenotypeRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Clinical Dysmorphology|April 5, 2016
A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring-Opitz syndromeGautham Arunachal, Sumita Danda, Sabita Omprakash, et al.
European Journal of Medical Genetics|August 3, 2018
A family with floppy neonates with severe respiratory insufficiency: A lethal phenotype of RFT1-CDG due to a novel mutationThangaraj Abiramalatha, Gautham Arunachal, Karthik Muthusamy, et al.
Indian Journal of Pediatrics|June 15, 2019
Genomics and Radiogenomics in Inherited Neurometabolic Disorders - A Practical Primer for PediatriciansSniya Valsa Sudhakar, Karthik Muthusamy, Gautham Arunachal, et al.
Indian Journal of Psychiatry|February 13, 2019
Clinical Practice Guidelines for Assessment and Management of intellectual disabilityM Thomas Kishore, Gautham Arunachal Udipi, Shekhar P Seshadri
Scientific Reports|May 24, 2017
Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohortNikhat Khan, Anuja Lipsa, Gautham Arunachal, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|October 25, 2024
Adult-Onset EIF2B-Pathies: A Clinical, Imaging and Genetic Profiling with Literature ReviewSangeeth Thuppanattumadam Ananthasubramanian, Gautham Arunachal, Hansashree Padmanabha, et al.
Pageof 13