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

Haematologica, Volume 108, Issue 1 by Haematologica - Issuu

Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI

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

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

Neelam GIRI, National Institutes of Health, MD, NIH

The genetics and clinical manifestations of telomere biology disorders - ScienceDirect

Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromes - Giri - 2018 - Pediatric Blood & Cancer - Wiley Online Library

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

Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect

The Unique Role of Staff Clinicians in DCEG Research - NCI