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Frenny Sheth

Showing results (51-60 of 67) 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 Human Genetics : EJHG|February 14, 2013
Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disabilityReza Asadollahi, Beatrice Oneda, Frenny Sheth, 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.
Genetics in Medicine Open|May 28, 2026
Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencingMei Ling Chong, Bruna Burssed, Chen Zhao, 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 Assisted Reproduction and Genetics|January 3, 2026
Genetic diversity of infertile males in IndiaHarsh Sheth, Pritti Priya, Vineet Mishra, et al.
Orphanet Journal of Rare Diseases|September 2, 2025
Prenatal diagnosis of rare genetic disorders: fourteen years' experience of a tertiary genetic centre from IndiaJayesh Sheth, Tejasvi Dhondekar, Manali Ajagekar, et al.
BMC Medical Genetics|February 16, 2019
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutationJayesh Sheth, Riddhi Bhavsar, Mehul Mistri, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
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 Human Genetics : EJHG|February 14, 2013
Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disabilityReza Asadollahi, Beatrice Oneda, Frenny Sheth, 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.
Genetics in Medicine Open|May 28, 2026
Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencingMei Ling Chong, Bruna Burssed, Chen Zhao, 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 Assisted Reproduction and Genetics|January 3, 2026
Genetic diversity of infertile males in IndiaHarsh Sheth, Pritti Priya, Vineet Mishra, et al.
Orphanet Journal of Rare Diseases|September 2, 2025
Prenatal diagnosis of rare genetic disorders: fourteen years' experience of a tertiary genetic centre from IndiaJayesh Sheth, Tejasvi Dhondekar, Manali Ajagekar, et al.
BMC Medical Genetics|February 16, 2019
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutationJayesh Sheth, Riddhi Bhavsar, Mehul Mistri, et al.
Pageof 7