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.

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

Neelam GIRI, National Institutes of Health, MD, NIH

News Fanconi Anemia Research Fund

Neelam GIRI, National Institutes of Health, MD, NIH

British Journal of Haematology

Dr. Neelam Giri, MD – Rockville, MD

The Unique Role of Staff Clinicians in DCEG Research - NCI

Blanche Alter Retires after 21 Years at NCI - NCI

The Unique Role of Staff Clinicians in DCEG Research - NCI

Molecular Hematopoiesis

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

Cells, Free Full-Text

Dr. Neelam Giri, MD - Pediatrics Specialist in Rockville, MD

Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature review, BMC Hematology

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