Ishwar C. Verma-Chander
New Delhi, DL 110060, India
Last Updated: 09/26/2026
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Found 15 publications
The molecular landscape of oculocutaneous albinism in India and its therapeutic implications.
Journal: European journal of human genetics : EJHG
Published: July 29, 2023
Neuro-Regression in a Child with Silvery Hair.
Journal: Indian journal of pediatrics
Published: April 24, 2020
NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot study.
Journal: BMC medical genetics
Published: April 17, 2020
Unique skeletal manifestations in patients with Primrose syndrome.
Journal: European journal of medical genetics
Published: March 25, 2020
Hypophosphatemic Rickets with R179W Mutation in FGFR23 Gene - A Rare But Treatable Cause of Refractory Rickets.
Journal: Indian journal of pediatrics
Published: March 20, 2020
Genetic Testing in Pediatric Kidney Disease.
Journal: Indian journal of pediatrics
Published: December 09, 2019
Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy.
Journal: Indian journal of pediatrics
Published: October 22, 2019
Genetic analysis of familial hypercholesterolemia in Asian Indians: A single-center study.
Journal: Journal of clinical lipidology
Published: June 26, 2019
Prevalence of familial hypercholesterolemia in premature coronary artery disease patients admitted to a tertiary care hospital in North India.
Journal: Indian heart journal
Published: October 27, 2018
Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD.
Journal: Journal of human genetics
Published: October 17, 2018
Fetal valproate syndrome as a phenocopy of Kleefstra syndrome.
Journal: Birth defects research
Published: May 16, 2018
Last Updated: 09/26/2026