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.

Neelam GIRI, National Institutes of Health, MD, NIH

The Unique Role of Staff Clinicians in DCEG Research - NCI

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

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

Cells, Free Full-Text

Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect

British Journal of Haematology

Dr. Neelam Giri, MD – Rockville, MD

PDF) Preemptive Bone Marrow Transplantation and Event-Free Survival in Fanconi Anemia

Neelam GIRI, National Institutes of Health, MD, NIH