Manju S. Gorivale
Mumbai, MH, India
Last Updated: 09/26/2026
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Found 12 publications
When a synonymous mutation breaks the silence in a thalassaemia patient.
Journal: British journal of haematology
Published: May 16, 2023
Diagnostic challenges posed by a rare unstable hemoglobin variant Hb Southampton [HBB: c.320T → C] with pyrimidine 5' nucleotidase deficiency and the response to HU therapy.
Journal: Blood cells, molecules & diseases
Published: February 15, 2022
The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades.
Journal: Hemoglobin
Published: April 08, 2021
Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine.
Journal: Scientific reports
Published: February 28, 2021
Prevalence of globin gene modifiers encountered in fetuses during antenatal diagnosis of hemoglobinopathies.
Journal: International journal of laboratory hematology
Published: January 20, 2020
The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center.
Journal: International journal of laboratory hematology
Published: July 19, 2018
Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?
Journal: Annals of human genetics
Published: January 08, 2017
Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Journal: Molecular biology reports
Published: August 18, 2016
Five Rare β Globin Chain Hemoglobin Variants in India.
Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
Published: July 29, 2015
Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partner.
Journal: Prenatal diagnosis
Published: June 26, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026