Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI
Por um escritor misterioso
Descrição
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.
American Journal of Hematology, Blood Research Journal
British Journal of Haematology
Dr. Neelam Giri, MD – Rockville, MD
The genetics and clinical manifestations of telomere biology disorders - ScienceDirect
Cells, Free Full-Text
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort
Neelam GIRI, National Institutes of Health, MD, NIH
British Journal of Haematology
Molecular Hematopoiesis
Blanche Alter Retires after 21 Years at NCI - NCI
Neelam GIRI, National Institutes of Health, MD, NIH
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort
MUSC Department of Medicine 2018 Annual Report by MUSC Department of Medicine - Issuu
Germline mutation of MDM4, a major p53 regulator, in a familial syndrome of defective telomere maintenance
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