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Harsh Sheth

Showing results (31-40 of 46) with videos related to

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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.
Plos One|August 30, 2018
A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumoursLisa Redford, Ghanim Alhilal, Stephanie Needham, 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.
Human Mutation|September 1, 2019
Sequencing-based microsatellite instability testing using as few as six markers for high-throughput clinical diagnosticsRichard Gallon, Harsh Sheth, Christine Hayes, et al.
Acta Neuropathologica Communications|November 21, 2013
Identification of a neuronal transcription factor network involved in medulloblastoma developmentMaria Lastowska, Hani Al-Afghani, Haya H Al-Balool, et al.
Clinical Genetics|August 22, 2024
SCYL2-related autosomal recessive neurodevelopmental disorders: Arthrogryposis multiplex congenita-4 and beyond?Marlène Malbos, Gabriella Vera, Harsh Sheth, et al.
Plos One|February 10, 2018
Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populationsHarsh Sheth, Emma Northwood, Cornelia M Ulrich, et al.
Lancet (London, England)|June 15, 2020
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trialJohn Burn, Harsh Sheth, Faye Elliott, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
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.
Plos One|August 30, 2018
A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumoursLisa Redford, Ghanim Alhilal, Stephanie Needham, 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.
Human Mutation|September 1, 2019
Sequencing-based microsatellite instability testing using as few as six markers for high-throughput clinical diagnosticsRichard Gallon, Harsh Sheth, Christine Hayes, et al.
Acta Neuropathologica Communications|November 21, 2013
Identification of a neuronal transcription factor network involved in medulloblastoma developmentMaria Lastowska, Hani Al-Afghani, Haya H Al-Balool, et al.
Clinical Genetics|August 22, 2024
SCYL2-related autosomal recessive neurodevelopmental disorders: Arthrogryposis multiplex congenita-4 and beyond?Marlène Malbos, Gabriella Vera, Harsh Sheth, et al.
Plos One|February 10, 2018
Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populationsHarsh Sheth, Emma Northwood, Cornelia M Ulrich, et al.
Lancet (London, England)|June 15, 2020
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trialJohn Burn, Harsh Sheth, Faye Elliott, et al.
Pageof 5