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Jayesh Sheth

Showing results (41-50 of 80) with videos related to

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Clinical Diabetes and Endocrinology|July 14, 2017
The association of dyslipidemia and obesity with glycated hemoglobinJayesh Sheth, Ankna Shah, Frenny Sheth, et al.
BMC Pregnancy and Childbirth|April 18, 2015
Prenatal screening of cytogenetic anomalies - a Western Indian experienceFrenny Sheth, Mizanur Rahman, Thomas Liehr, 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.
Molecular Biology Reports|February 2, 2021
Giant axonal neuropathy with novel GAN pathogenic variant in a patient of consanguineous origin from Poonch Jammu and Kashmir-IndiaYaser Rafiq Mir, Xue Zeng, Atul K Taneja, 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.
Molecular Cytogenetics|November 2, 2017
Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15Stuti Tewari, Naznin Lubna, Raju Shah, et al.
Fertility and Sterility|May 26, 2009
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertilityGiovanna Vinci, Raja Brauner, Attila Tar, et al.
BMC Medical Genetics|October 5, 2018
Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in IndiaJayesh Sheth, Dhairya Pancholi, Mehul Mistri, et al.
Plos One|June 23, 2012
Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from IndiaMehul Mistri, Parag M Tamhankar, Frenny Sheth, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Expanding the spectrum of <i>HEXA</i> mutations in Indian patients with Tay-Sachs diseaseJayesh Sheth, Mehul Mistri, Chaitanya Datar, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Clinical Diabetes and Endocrinology|July 14, 2017
The association of dyslipidemia and obesity with glycated hemoglobinJayesh Sheth, Ankna Shah, Frenny Sheth, et al.
BMC Pregnancy and Childbirth|April 18, 2015
Prenatal screening of cytogenetic anomalies - a Western Indian experienceFrenny Sheth, Mizanur Rahman, Thomas Liehr, 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.
Molecular Biology Reports|February 2, 2021
Giant axonal neuropathy with novel GAN pathogenic variant in a patient of consanguineous origin from Poonch Jammu and Kashmir-IndiaYaser Rafiq Mir, Xue Zeng, Atul K Taneja, 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.
Molecular Cytogenetics|November 2, 2017
Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15Stuti Tewari, Naznin Lubna, Raju Shah, et al.
Fertility and Sterility|May 26, 2009
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertilityGiovanna Vinci, Raja Brauner, Attila Tar, et al.
BMC Medical Genetics|October 5, 2018
Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in IndiaJayesh Sheth, Dhairya Pancholi, Mehul Mistri, et al.
Plos One|June 23, 2012
Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from IndiaMehul Mistri, Parag M Tamhankar, Frenny Sheth, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Expanding the spectrum of <i>HEXA</i> mutations in Indian patients with Tay-Sachs diseaseJayesh Sheth, Mehul Mistri, Chaitanya Datar, et al.
Pageof 8