Dhaval I. Solanki
Bhavnagar, UP, India
Last Updated: 09/26/2026
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Found 8 publications
Development of national biobank for lysosomal storage disorders in India- a step towards advancing research and precision medicine.
Journal: Orphanet journal of rare diseases
Published: October 31, 2025
Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.
Journal: Orphanet journal of rare diseases
Published: April 18, 2024
Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India.
Journal: Human genomics
Published: March 05, 2024
Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test.
Journal: BMC neurology
Published: May 18, 2023
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.
Journal: Journal of pediatric genetics
Published: May 06, 2020
Identification of novel variants in a large cohort of children with Tay-Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India.
Journal: Journal of human genetics
Published: October 15, 2018
A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature.
Journal: Italian journal of pediatrics
Published: August 04, 2018
Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India.
Journal: BMC medical genetics
Published: October 26, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026