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Jayesh Sheth

Showing results (11-20 of 80) with videos related to

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Journal of Clinical Ultrasound : JCU|December 11, 2007
Early antenatal diagnosis of spina bifida presenting with a "step" in the posterior contour of an 8-week embryoChander Lulla, Amogh Hegde, Jatin Shah, et al.
Indian Pediatrics|April 6, 2004
Lysosomal storage disordersJayesh Sheth, Pinaki Patel, Frenny Sheth, et al.
The Indian Journal of Medical Research|September 20, 2022
Rapid molecular identification of a rare <i>β-globin</i> gene deletion & its clinical implicationPriya Hariharan, Pratibha Sawant, Jayesh Sheth, et al.
Movement Disorders Clinical Practice|July 7, 2020
A Case Report of Chronic Progressive Pancerebellar Syndrome with Leukoencephalopathy:L-2 Hydroxyglutaric AciduriaHeli Shah, Mitesh Chandarana, Jayesh Sheth, et al.
Indian Pediatrics|December 21, 2012
Clinical and molecular characterization of patients with gross hypotonia and impaired lower motor neuron functionJayesh Sheth, Harsh Patel, Sanjiv Mehta, et al.
BMC Medical Genetics|May 13, 2018
A case of Raine syndrome presenting with facial dysmorphy and review of literatureJayesh Sheth, Riddhi Bhavsar, Ajit Gandhi, et al.
Indian Pediatrics|November 14, 2007
Cytogenetic analysis of Down syndrome in GujaratFrenny Sheth, Subhada Rao, Manisha Desai, et al.
Frontiers in Genetics|October 15, 2021
Case Report: Recurrent Variant c.298 TA in <i>CCN6</i> Gene Found in Progressive Pseudorheumatoid Dysplasia Patients From Patni Community of Gujarat: A Report of Three CasesHarsh Sheth, Jhanvi Shah, Aadhira Nair, et al.
International Journal of Dermatology|August 1, 2015
Novel mutation in the XPC gene: a case report of a patient with xeroderma pigmentosumJayesh Sheth, Mehul Mistri, Riddhi Bhavsar, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Novel LINS1 missense mutation in a family with non-syndromic intellectual disabilityJayesh Sheth, Gyan Ranjan, Krati Shah, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Journal of Clinical Ultrasound : JCU|December 11, 2007
Early antenatal diagnosis of spina bifida presenting with a "step" in the posterior contour of an 8-week embryoChander Lulla, Amogh Hegde, Jatin Shah, et al.
Indian Pediatrics|April 6, 2004
Lysosomal storage disordersJayesh Sheth, Pinaki Patel, Frenny Sheth, et al.
The Indian Journal of Medical Research|September 20, 2022
Rapid molecular identification of a rare <i>β-globin</i> gene deletion & its clinical implicationPriya Hariharan, Pratibha Sawant, Jayesh Sheth, et al.
Movement Disorders Clinical Practice|July 7, 2020
A Case Report of Chronic Progressive Pancerebellar Syndrome with Leukoencephalopathy:L-2 Hydroxyglutaric AciduriaHeli Shah, Mitesh Chandarana, Jayesh Sheth, et al.
Indian Pediatrics|December 21, 2012
Clinical and molecular characterization of patients with gross hypotonia and impaired lower motor neuron functionJayesh Sheth, Harsh Patel, Sanjiv Mehta, et al.
BMC Medical Genetics|May 13, 2018
A case of Raine syndrome presenting with facial dysmorphy and review of literatureJayesh Sheth, Riddhi Bhavsar, Ajit Gandhi, et al.
Indian Pediatrics|November 14, 2007
Cytogenetic analysis of Down syndrome in GujaratFrenny Sheth, Subhada Rao, Manisha Desai, et al.
Frontiers in Genetics|October 15, 2021
Case Report: Recurrent Variant c.298 TA in <i>CCN6</i> Gene Found in Progressive Pseudorheumatoid Dysplasia Patients From Patni Community of Gujarat: A Report of Three CasesHarsh Sheth, Jhanvi Shah, Aadhira Nair, et al.
International Journal of Dermatology|August 1, 2015
Novel mutation in the XPC gene: a case report of a patient with xeroderma pigmentosumJayesh Sheth, Mehul Mistri, Riddhi Bhavsar, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Novel LINS1 missense mutation in a family with non-syndromic intellectual disabilityJayesh Sheth, Gyan Ranjan, Krati Shah, et al.
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