Alec E. Correa
New Delhi, DL, India
Last Updated: 09/26/2026
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Found 8 publications
The spectrum of neurological manifestations and genotype-phenotype correlation in Indian children with Gaucher disease.
Journal: American journal of medical genetics. Part A
Published: September 29, 2022
First case report of Penttinen syndrome from India.
Journal: American journal of medical genetics. Part A
Published: May 30, 2021
Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum.
Journal: Annals of human genetics
Published: September 19, 2020
Mevalonate Kinase Deficiency as Cause of Periodic Fever in Two Siblings.
Journal: Indian pediatrics
Published: February 16, 2020
Methylene Tetrahydrofolate Reductase Deficiency.
Journal: Indian journal of pediatrics
Published: February 09, 2020
Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases.
Journal: Indian journal of pediatrics
Published: August 06, 2019
Report of a Novel Homozygous Nonsense DDR2 Mutation in an Indian Adult Male with Spondylo-meta-epiphyseal Dysplasia, Short Limb-Abnormal Calcification Type.
Journal: Journal of pediatric genetics
Published: October 07, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026