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.

Molecular Hematopoiesis

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

Neelam GIRI, National Institutes of Health, MD, NIH

Neelam GIRI, National Institutes of Health, MD, NIH

British Journal of Haematology

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

News Fanconi Anemia Research Fund

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