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Harsh Sheth

Showing results (11-20 of 46) with videos related to

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Obesity Surgery|April 25, 2019
The HAALT Non-invasive Scoring System for NAFLD in ObesityHarsh Sheth, Samir Bagasrawala, Mita Shah, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|November 19, 2025
Trends, case selection and comparative outcomes of e-TEP with TAPP and TEP for groin hernia - data from Indian hernia collaborativeSarfaraz Baig, Harsh Sheth, Magan Mehrotra, et al.
BMC Pediatrics|February 4, 2022
An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene: a case reportShruti Bajaj, Purnima Satoskar, Aadhira Nair, et al.
BMC Neurology|January 16, 2023
A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case reportFrenny Sheth, Jhanvi Shah, Ketan Patel, et al.
BMC Medical Genomics|September 25, 2020
Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case reportHarsh Sheth, Sunil Trivedi, Thomas Liehr, et al.
Familial Cancer|December 20, 2024
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohortHarsh Sheth, Jyoti Sadhwani, Abhinav Jain, et al.
Journal of Assisted Reproduction and Genetics|November 14, 2024
Complex chromosomal rearrangements in female carriers experiencing recurrent pregnancy loss or poor obstetric history and literature reviewFrenny Sheth, Jhanvi Shah, Thomas Liehr, et al.
BMC Genomics|June 21, 2022
The GALNS p.P77R variant is a probable Gujarati-Indian founder mutation causing Mucopolysaccharidosis IVA syndromeHarsh Sheth, Premal Naik, Maulin Shah, et al.
Molecular Cytogenetics|July 3, 2013
Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qterFrenny Sheth, Joris Andrieux, Stuti Tewari, et al.
JIMD Reports|July 5, 2023
Late infantile and adult-onset metachromatic leukodystrophy due to novel missense variants in the <i>PSAP</i> gene: Case report from IndiaJayesh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Obesity Surgery|April 25, 2019
The HAALT Non-invasive Scoring System for NAFLD in ObesityHarsh Sheth, Samir Bagasrawala, Mita Shah, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|November 19, 2025
Trends, case selection and comparative outcomes of e-TEP with TAPP and TEP for groin hernia - data from Indian hernia collaborativeSarfaraz Baig, Harsh Sheth, Magan Mehrotra, et al.
BMC Pediatrics|February 4, 2022
An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene: a case reportShruti Bajaj, Purnima Satoskar, Aadhira Nair, et al.
BMC Neurology|January 16, 2023
A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case reportFrenny Sheth, Jhanvi Shah, Ketan Patel, et al.
BMC Medical Genomics|September 25, 2020
Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case reportHarsh Sheth, Sunil Trivedi, Thomas Liehr, et al.
Familial Cancer|December 20, 2024
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohortHarsh Sheth, Jyoti Sadhwani, Abhinav Jain, et al.
Journal of Assisted Reproduction and Genetics|November 14, 2024
Complex chromosomal rearrangements in female carriers experiencing recurrent pregnancy loss or poor obstetric history and literature reviewFrenny Sheth, Jhanvi Shah, Thomas Liehr, et al.
BMC Genomics|June 21, 2022
The GALNS p.P77R variant is a probable Gujarati-Indian founder mutation causing Mucopolysaccharidosis IVA syndromeHarsh Sheth, Premal Naik, Maulin Shah, et al.
Molecular Cytogenetics|July 3, 2013
Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qterFrenny Sheth, Joris Andrieux, Stuti Tewari, et al.
JIMD Reports|July 5, 2023
Late infantile and adult-onset metachromatic leukodystrophy due to novel missense variants in the <i>PSAP</i> gene: Case report from IndiaJayesh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.
Pageof 5