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Jayesh Sheth

Showing results (1-10 of 80) with videos related to

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Molecular Cytogenetics|June 19, 2014
Molecular study of lysosomal storage disorders in IndiaJayesh Sheth
The Indian Journal of Medical Research|October 12, 2011
Umbilical cord blood: current status & promise for the futureDavid McKenna, Jayesh Sheth
Current Pharmaceutical Design|October 16, 2020
Treatment for Lysosomal Storage DisordersJayesh Sheth, Aadhira Nair
Indian Pediatrics|July 31, 2002
Prenatal diagnosis of tay-sachs b1 variant in a maharashtrian familyJayesh Sheth, Raktima Bhattacharya, Frenny Sheth
Indian Journal of Pediatrics|May 29, 2007
Ring chromosome 9 in a dysmorphic childJayesh Sheth, Rajesh Joshi, Frenny Sheth
The Lancet Regional Health. Southeast Asia|June 29, 2023
Lysosomal storage disorders: from biology to the clinic with reference to IndiaJayesh Sheth, Aadhira Nair, Babban Jee
Indian Pediatrics|April 8, 2010
Supernumerary marker chromosome in a child with microcephaly and mental retardationFrenny Sheth, Joris Andrieux, Jayesh Sheth
Molecular Cytogenetics|July 24, 2015
Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocationFrenny Sheth, Thomas Liehr, Krati Shah, et al.
Molecular Biology Reports|May 18, 2011
STR markers for detecting heterogeneity in Indian populationShalu Jain, Inusha Panigrahi, Jayesh Sheth, et al.
Pediatrics and Neonatology|January 31, 2024
Non-immune hydrops fetalis due to infantile sialidosisInusha Panigrahi, Sudhanshu Grover, Mahesh Hiranandani, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Molecular Cytogenetics|June 19, 2014
Molecular study of lysosomal storage disorders in IndiaJayesh Sheth
The Indian Journal of Medical Research|October 12, 2011
Umbilical cord blood: current status & promise for the futureDavid McKenna, Jayesh Sheth
Current Pharmaceutical Design|October 16, 2020
Treatment for Lysosomal Storage DisordersJayesh Sheth, Aadhira Nair
Indian Pediatrics|July 31, 2002
Prenatal diagnosis of tay-sachs b1 variant in a maharashtrian familyJayesh Sheth, Raktima Bhattacharya, Frenny Sheth
Indian Journal of Pediatrics|May 29, 2007
Ring chromosome 9 in a dysmorphic childJayesh Sheth, Rajesh Joshi, Frenny Sheth
The Lancet Regional Health. Southeast Asia|June 29, 2023
Lysosomal storage disorders: from biology to the clinic with reference to IndiaJayesh Sheth, Aadhira Nair, Babban Jee
Indian Pediatrics|April 8, 2010
Supernumerary marker chromosome in a child with microcephaly and mental retardationFrenny Sheth, Joris Andrieux, Jayesh Sheth
Molecular Cytogenetics|July 24, 2015
Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocationFrenny Sheth, Thomas Liehr, Krati Shah, et al.
Molecular Biology Reports|May 18, 2011
STR markers for detecting heterogeneity in Indian populationShalu Jain, Inusha Panigrahi, Jayesh Sheth, et al.
Pediatrics and Neonatology|January 31, 2024
Non-immune hydrops fetalis due to infantile sialidosisInusha Panigrahi, Sudhanshu Grover, Mahesh Hiranandani, et al.
Pageof 8