Sona B. Nair
Mumbai, MH, India
Last Updated: 09/26/2026
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Found 9 publications
First Report of an α Chain Variant [Hb Coombe Park (HBA2: c.382A>G)] from India, Coinherited with a Novel SERPINC1 Gene Mutation: A Double Whammy?
Journal: Hemoglobin
Published: September 19, 2022
Detection of a novel mutation in NLRP3/CIAS1 gene in an Indian child with Neonatal-Onset Multisystem Inflammatory Disease (NOMID).
Journal: Clinical rheumatology
Published: March 27, 2018
Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.
Journal: PloS one
Published: March 26, 2014
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India.
Journal: Indian journal of human genetics
Published: December 17, 2013
Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from India.
Journal: Hematology (Amsterdam, Netherlands)
Published: October 01, 2013
Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal A T(Indian) (AATAAA>AATA- -) mutation in four Indian families.
Journal: Hemoglobin
Published: March 23, 2013
SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India.
Journal: Indian journal of human genetics
Published: July 04, 2012
First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
Journal: Journal of clinical pathology
Published: March 31, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026