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.

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

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

Neelam GIRI, National Institutes of Health, MD, NIH

The genetics and clinical manifestations of telomere biology disorders - ScienceDirect

Cells, Free Full-Text

British Journal of Haematology

Dr. Neelam Giri, MD – Rockville, MD

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

Dr. Neelam Giri, MD – Rockville, MD

Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders - The Journal of Pediatrics