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.

The incidence and spectrum of congenital hand differences in patients with Fanconi anaemia: analysis of 48 patients - Grainne Bourke, Daniel Wilks, Sally Kinsey, Richard G. Feltbower, Neelam Giri, Blanche P. Alter, 2022

Neelam GIRI, National Institutes of Health, MD, NIH

Neelam GIRI, National Institutes of Health, MD, NIH

Germline mutation of MDM4, a major p53 regulator, in a familial syndrome of defective telomere maintenance

Haematologica, Volume 108, Issue 1 by Haematologica - Issuu

British Journal of Haematology

Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect

Molecular Hematopoiesis

Cells, Free Full-Text

Neelam GIRI, National Institutes of Health, MD, NIH

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