Veronica Arora

New Delhi, DL, India

Last Updated: 09/26/2026

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Found 39 publications

Position Statement of the Indian Academy of Medical Genetics on Cytogenetic and Molecular Cytogenetic Testing.

Position Statement of the Indian Academy of Medical Genetics on Cytogenetic and Molecular Cytogenetic Testing.

Journal: Indian journal of pediatrics

Published: February 22, 2026

Organic Acidemias in India: Clinical and Molecular Spectrum.

Organic Acidemias in India: Clinical and Molecular Spectrum.

Journal: Indian journal of pediatrics

Published: December 22, 2025

Binder Phenotype: Evaluating the Utility and Influence of Genetic Results on Parental Decision Making in Antenatally Diagnosed Cases.

Binder Phenotype: Evaluating the Utility and Influence of Genetic Results on Parental Decision Making in Antenatally Diagnosed Cases.

Journal: American journal of medical genetics. Part A

Published: June 02, 2025

Unusual Dual Fungal Infection in STAT1 Gain-of-Function CMC: Clinical and Mycological Insights.

Unusual Dual Fungal Infection in STAT1 Gain-of-Function CMC: Clinical and Mycological Insights.

Journal: International journal of dermatology

Published: May 15, 2025

Molecular Landscape of Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency in India.

Molecular Landscape of Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency in India.

Journal: Indian journal of pediatrics

Published: March 03, 2025

The molecular landscape of oculocutaneous albinism in India and its therapeutic implications.

The molecular landscape of oculocutaneous albinism in India and its therapeutic implications.

Journal: European journal of human genetics : EJHG

Published: July 29, 2023

Clinical Remission of Immunoglobulin A Nephropathy after Bariatric Surgery in a Young Morbidly Obese Patient.

Clinical Remission of Immunoglobulin A Nephropathy after Bariatric Surgery in a Young Morbidly Obese Patient.

Journal: Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

Published: August 10, 2022

CDKN1C -Related Beckwith-Wiedemann Syndrome: First Patient from India.

CDKN1C -Related Beckwith-Wiedemann Syndrome: First Patient from India.

Journal: Journal of pediatric genetics

Published: March 16, 2022

Fragile X Syndrome Due to a Frameshift Deletion: A Rare Mechanism.

Fragile X Syndrome Due to a Frameshift Deletion: A Rare Mechanism.

Journal: Indian journal of pediatrics

Published: February 14, 2022

Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene.

Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene.

Journal: Indian journal of pediatrics

Published: December 15, 2021

Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up.

Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up.

Journal: Journal of clinical imaging science

Published: December 08, 2021

Risk factors for Coronavirus disease-associated mucormycosis.

Risk factors for Coronavirus disease-associated mucormycosis.

Journal: The Journal of infection

Published: September 11, 2021

Showing 1-12 of 39

Last Updated: 09/26/2026