Rapid molecular identification of a rare β-globin gene deletion & its clinical implication

por Hariharan, Priya, Sawant, Pratibha, Sheth, Jayesh, Nadkarni, Anita
Publicado 2022

Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine

por Hariharan, Priya, Gorivale, Manju, Sawant, Pratibha, Mehta, Pallavi, Nadkarni, Anita
Publicado 2021

HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association

por Colaco, Stacy, Surve, Reema, Sawant, Pratibha, Nadkarni, Anita, Ghosh, Kanjaksha, Colah, Roshan
Publicado 2014

Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India

por Mashon, Ranjeet Singh, Nair, Sona, Sawant, Pratibha, Colah, Roshan B., Ghosh, Kanjaksha, Das, Sheila
Publicado 2013