Usha P. Dave
Mumbai, MH, India
Last Updated: 09/26/2026
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Found 8 publications
Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort.
Journal: Indian journal of clinical biochemistry : IJCB
Published: November 24, 2023
Hemoglobin Variant Analysis and Its Comparison between Conventional High-performance Liquid Chromatography Using Whole Blood versus Dried Blood Spot: High-performance Liquid Chromatography.
Journal: Indian journal of public health
Published: August 11, 2023
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Journal: American journal of medical genetics. Part A
Published: March 23, 2023
Cornelia de Lange syndrome in diverse populations.
Journal: American journal of medical genetics. Part A
Published: June 05, 2018
Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency.
Journal: JIMD reports
Published: July 28, 2016
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.
Journal: Journal of human genetics
Published: May 27, 2015
Brain-Derived Neurotrophic Factor in children with Autism Spectrum Disorder.
Journal: Annals of neurosciences
Published: April 09, 2014
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.
Journal: Journal of human genetics
Published: November 27, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026