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Veronica Arora

8PUBLICATIONS
8CO-AUTHORS
Neurology and neuromuscular diseasesFree radical chemistryEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsCancer genetics
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Journal

Publications (8)

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|Aug 04, 2022
Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene.

Aashita Takkar, Veronica Arora, Renu Saxena

|Jul 20, 2022
Fragile X Syndrome Due to a Frameshift Deletion: A Rare Mechanism.

Veronica Arora, Aashita Takkar, Ashima Mehta

|Oct 22, 2020
Genetic Testing in Pediatric Epilepsy.

Ishwar C Verma, Sameer Bhatia, Veronica Arora

|Oct 06, 2020
Biallelic Pathogenic <i>GFRA1</i> Variants Cause Autosomal Recessive Bilateral Renal Agenesis.

Veronica Arora, Suliman Khan, Ayman W El-Hattab

|Mar 05, 2020
Expanding the phenotypic and genotypic spectrum of Wiedemann-Steiner syndrome: First patient from India.

Veronica Arora, Ratna D Puri, Sunita Bijarnia-Mahay

|Oct 24, 2019
Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation.

Veronica Arora, Sunita Bijarnia-Mahay, Samarth Kulshreshtra

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Frequent Collaborators

3 joint publications

Ratna Dua Puri

3 joint publications

Ishwar Chandar Verma

1 joint publications

Sunita Bijarnia-Mahay

1 joint publications

Samarth Kulshreshtra

1 joint publications

Kanika Singh

1 joint publications

Ayman W El-Hattab

1 joint publications

Rijad Merdzanic

1 joint publications

Sameer Bhatia

Frequent Collaborators

3 joint publications

Ratna Dua Puri

3 joint publications

Ishwar Chandar Verma

1 joint publications

Sunita Bijarnia-Mahay

1 joint publications

Samarth Kulshreshtra

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