Sridevi Hegde

Airport Road
Bengaluru, KA 560017, India

Last Updated: 09/26/2026

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Found 10 publications

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome.

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome.

Journal: Journal of visualized experiments : JoVE

Published: December 20, 2021

Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India.

Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: July 05, 2019

Sporadic spinocerebellar ataxia, type 5: First report from India.

Sporadic spinocerebellar ataxia, type 5: First report from India.

Journal: Neurology India

Published: January 12, 2018

Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in India.

Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in India.

Journal: Journal of obstetrics and gynaecology of India

Published: September 08, 2017

A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders.

A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders.

Journal: Molecular syndromology

Published: June 26, 2017

Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.

Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.

Journal: Cytogenetic and genome research

Published: February 15, 2016

Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease.

Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease.

Journal: Indian journal of pediatrics

Published: January 13, 2016

Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.

Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.

Journal: Molecular syndromology

Published: November 09, 2015

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.

Journal: Molecular syndromology

Published: August 17, 2015

The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population.

The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population.

Journal: Pediatric cardiology

Published: December 22, 2014

Showing 1-10 of 10

Last Updated: 09/26/2026