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Journal of Human Genetics
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May 27, 2015
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
Chitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
European Journal of Medical Genetics
|
February 15, 2011
Characterization of sSMC by FISH and molecular techniques
Frenny Sheth, Joris Andrieux, Elisabeth Ewers, et al.
Journal of Human Genetics
|
February 14, 2014
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
Chitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
Molecular Cytogenetics
|
June 21, 2014
Point of care testing for improving risk- benefit ratio of aspirin and warfarin
Harsh Sheth, Emma Northwood, Faye Elliott, et al.
BMC Pediatrics
|
June 27, 2026
Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India
Jayesh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.
Orphanet Journal of Rare Diseases
|
April 18, 2020
Natural history of non-lethal Raine syndrome during childhood
Chiara Mameli, Giulia Zichichi, Nasim Mahmood, et al.
American Journal of Medical Genetics. Part A
|
October 15, 2024
KBG Syndrome in 16 Indian Individuals
Shruti 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 test
Frenny Sheth, Jhanvi Shah, Deepika Jain, et al.
Journal of Pediatric Genetics
|
September 10, 2021
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1
Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, et al.
Journal of Assisted Reproduction and Genetics
|
January 3, 2026
Genetic diversity of infertile males in India
Harsh Sheth, Pritti Priya, Vineet Mishra, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 80) with videos related to
Sort By:
Page
of 8
Journal of Human Genetics
|
May 27, 2015
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
Chitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
European Journal of Medical Genetics
|
February 15, 2011
Characterization of sSMC by FISH and molecular techniques
Frenny Sheth, Joris Andrieux, Elisabeth Ewers, et al.
Journal of Human Genetics
|
February 14, 2014
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
Chitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, et al.
Molecular Cytogenetics
|
June 21, 2014
Point of care testing for improving risk- benefit ratio of aspirin and warfarin
Harsh Sheth, Emma Northwood, Faye Elliott, et al.
BMC Pediatrics
|
June 27, 2026
Clinical, biochemical and molecular spectrum of acute neuronopathic type 2 Gaucher disease from India
Jayesh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.
Orphanet Journal of Rare Diseases
|
April 18, 2020
Natural history of non-lethal Raine syndrome during childhood
Chiara Mameli, Giulia Zichichi, Nasim Mahmood, et al.
American Journal of Medical Genetics. Part A
|
October 15, 2024
KBG Syndrome in 16 Indian Individuals
Shruti 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 test
Frenny Sheth, Jhanvi Shah, Deepika Jain, et al.
Journal of Pediatric Genetics
|
September 10, 2021
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1
Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, et al.
Journal of Assisted Reproduction and Genetics
|
January 3, 2026
Genetic diversity of infertile males in India
Harsh Sheth, Pritti Priya, Vineet Mishra, et al.
Page
of 8