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.

Dr. Neelam Giri, MD – Rockville, MD

Proceedings of a Workshop, Companion Animals as Sentinels for Predicting Environmental Exposure Effects on Aging and Cancer Susceptibility in Humans: Proceedings of a Workshop

Neelam GIRI, National Institutes of Health, MD, NIH

Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort

Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort

British Journal of Haematology

Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort

Neelam GIRI, National Institutes of Health, MD, NIH

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

The Unique Role of Staff Clinicians in DCEG Research - NCI

Neelam GIRI, National Institutes of Health, MD, NIH

Dr. Neelam Giri, MD – Rockville, MD

British Journal of Haematology