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American Journal of Medical Genetics. Part A|March 31, 2016
Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOSBlanche P Alter, Neelam Giri
British Journal of Haematology|February 22, 2022
Fanconi anaemia: A syndrome with distinct subgroupsBlanche P Alter, Neelam Giri, Lisa J McReynolds, et al.
British Journal of Haematology|July 30, 2013
Cytokine production by bone marrow mononuclear cells in inherited bone marrow failure syndromesKen Matsui, Neelam Giri, Blanche P Alter, et al.
Hematology (Amsterdam, Netherlands)|December 12, 2003
Persistent questions about the treatment of severe aplastic anemia in children as illustrated by five casesMichael E Trigg, Robert Bond, Neelam Giri, et al.
Frontiers in Genetics|August 4, 2022
Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19Sarah Cole, Neelam Giri, Blanche P Alter, et al.
British Journal of Haematology|May 21, 2021
Gynaecological and reproductive health of women with telomere biology disordersNeelam Giri, Blanche P Alter, Sharon A Savage, et al.
Haematologica|October 21, 2017
Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-upBlanche P Alter, Neelam Giri, Sharon A Savage, et al.
Clinical Genetics|August 5, 2025
Avascular Necrosis and Minimal Trauma Fractures in Telomere Biology DisordersArman M Niknafs, Neelam Giri, Marena R Niewisch, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2007
Endocrine abnormalities in patients with Fanconi anemiaNeelam Giri, Dalia L Batista, Blanche P Alter, et al.
Blood|March 14, 2009
Cancer in dyskeratosis congenitaBlanche P Alter, Neelam Giri, Sharon A Savage, et al.
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