Sunita B. Mahay

New Delhi, DL, India

Last Updated: 09/26/2026

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Found 10 publications

Expanding the Malignancy Spectrum of Tatton-Brown-Rahman Syndrome: A Case of Hodgkin Lymphoma.

Expanding the Malignancy Spectrum of Tatton-Brown-Rahman Syndrome: A Case of Hodgkin Lymphoma.

Journal: Pediatric blood & cancer

Published: October 31, 2025

Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of 300 Indian Patients.

Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of 300 Indian Patients.

Journal: Indian journal of pediatrics

Published: December 22, 2023

Decoding the Genetics of Recurrent Molar Pregnancy.

Decoding the Genetics of Recurrent Molar Pregnancy.

Journal: Journal of human reproductive sciences

Published: September 20, 2023

Next-Generation Sequencing in Unexplained Intellectual Disability.

Next-Generation Sequencing in Unexplained Intellectual Disability.

Journal: Indian journal of pediatrics

Published: December 11, 2022

Antenatal Phenotype of Desbuquois Dysplasia.

Antenatal Phenotype of Desbuquois Dysplasia.

Journal: Indian journal of pediatrics

Published: September 07, 2022

Clinico-radiological and biochemical clues to early diagnosis of mucolipidosis type II.

Clinico-radiological and biochemical clues to early diagnosis of mucolipidosis type II.

Journal: Clinical dysmorphology

Published: September 25, 2021

Prenatal phenotypic spectrum of full trisomy 18 in an Indian cohort.

Prenatal phenotypic spectrum of full trisomy 18 in an Indian cohort.

Journal: American journal of medical genetics. Part A

Published: December 26, 2020

Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.

Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.

Journal: Indian journal of dermatology

Published: April 16, 2019

Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India.

Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India.

Journal: Indian pediatrics

Published: April 08, 2019

Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase Deficiency.

Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase Deficiency.

Journal: Annals of Indian Academy of Neurology

Published: August 22, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026