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Jayesh Sheth

Showing results (61-70 of 80) with videos related to

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Journal of Human Genetics|May 27, 2015
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher diseaseChitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
European Journal of Medical Genetics|February 15, 2011
Characterization of sSMC by FISH and molecular techniquesFrenny Sheth, Joris Andrieux, Elisabeth Ewers, et al.
Journal of Human Genetics|February 14, 2014
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher diseaseChitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
Molecular Cytogenetics|June 21, 2014
Point of care testing for improving risk- benefit ratio of aspirin and warfarinHarsh Sheth, Emma Northwood, Faye Elliott, et al.
BMC Pediatrics|June 27, 2026
Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from IndiaJayesh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.
Orphanet Journal of Rare Diseases|April 18, 2020
Natural history of non-lethal Raine syndrome during childhoodChiara Mameli, Giulia Zichichi, Nasim Mahmood, et al.
American Journal of Medical Genetics. Part A|October 15, 2024
KBG Syndrome in 16 Indian IndividualsShruti Bajaj, Sheela Nampoothiri, Roshni Chugh, et al.
BMC Neurology|August 5, 2023
Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier testFrenny Sheth, Jhanvi Shah, Deepika Jain, et al.
Journal of Pediatric Genetics|September 10, 2021
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, et al.
Journal of Assisted Reproduction and Genetics|January 3, 2026
Genetic diversity of infertile males in IndiaHarsh Sheth, Pritti Priya, Vineet Mishra, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Journal of Human Genetics|May 27, 2015
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher diseaseChitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
European Journal of Medical Genetics|February 15, 2011
Characterization of sSMC by FISH and molecular techniquesFrenny Sheth, Joris Andrieux, Elisabeth Ewers, et al.
Journal of Human Genetics|February 14, 2014
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher diseaseChitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
Molecular Cytogenetics|June 21, 2014
Point of care testing for improving risk- benefit ratio of aspirin and warfarinHarsh Sheth, Emma Northwood, Faye Elliott, et al.
BMC Pediatrics|June 27, 2026
Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from IndiaJayesh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.
Orphanet Journal of Rare Diseases|April 18, 2020
Natural history of non-lethal Raine syndrome during childhoodChiara Mameli, Giulia Zichichi, Nasim Mahmood, et al.
American Journal of Medical Genetics. Part A|October 15, 2024
KBG Syndrome in 16 Indian IndividualsShruti Bajaj, Sheela Nampoothiri, Roshni Chugh, et al.
BMC Neurology|August 5, 2023
Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier testFrenny Sheth, Jhanvi Shah, Deepika Jain, et al.
Journal of Pediatric Genetics|September 10, 2021
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, et al.
Journal of Assisted Reproduction and Genetics|January 3, 2026
Genetic diversity of infertile males in IndiaHarsh Sheth, Pritti Priya, Vineet Mishra, et al.
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