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.

Haematologica, Volume 108, Issue 1 by Haematologica - Issuu

American Journal of Hematology, Blood Research Journal

Dr. Neelam Giri, MD – Rockville, MD

Molecular Hematopoiesis

Neelam GIRI, National Institutes of Health, MD, NIH

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

Neelam GIRI, National Institutes of Health, MD, NIH

MUSC Department of Medicine 2018 Annual Report by MUSC Department of Medicine - Issuu

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

News Fanconi Anemia Research Fund

Professor Sunil Lakhani - Centre for Clinical Research - University of Queensland

Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect

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