Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI

Dr. Neelam Giri conducts clinical and laboratory research focused on the various diseases that are being studied as part of the DCEG Inherited Bone Marrow Failure Syndromes Program, including Fanconi's anemia, dyskeratosis congenita, Diamond-Blackfan anemia and Shwachman-Diamond syndrome.

HBCR 2021

Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features. - Abstract - Europe PMC

Neelam GIRI, National Institutes of Health, MD, NIH

Neelam GIRI, National Institutes of Health, MD, NIH

Neelam GIRI, National Institutes of Health, MD, NIH

PDF) Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19

Frontiers Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19

Diverse Applications of Nanomedicine

Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features. - Abstract - Europe PMC

British Journal of Haematology

Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI

Secretary Azar and Doctors Fauci and Collins Receive COVID-19 Vaccine

Neelam GIRI, National Institutes of Health, MD, NIH

Joel Walker Fund Fanconi Anemia Research Fund

Frontiers Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19