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Blood|August 15, 2013
Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q- syndromeAdrianna Vlachos, Jason E Farrar, Eva Atsidaftos, et al.
Molecular Medicine (Cambridge, Mass.)|January 7, 2016
HMGB1 Mediates Anemia of Inflammation in Murine Sepsis SurvivorsSergio I Valdés-Ferrer, Julien Papoin, Meghan E Dancho, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 24, 2017
Late Effects Screening Guidelines after Hematopoietic Cell Transplantation for Inherited Bone Marrow Failure Syndromes: Consensus Statement From the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects After Pediatric HCTAndrew C Dietz, Sharon A Savage, Adrianna Vlachos, et al.
American Journal of Hematology|July 22, 2014
Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosisJason E Farrar, Paola Quarello, Ross Fisher, et al.
British Journal of Haematology|September 24, 2004
RNA and protein evidence for haplo-insufficiency in Diamond-Blackfan anaemia patients with RPS19 mutationsHanna T Gazda, Rong Zhong, Lilia Long, et al.
American Journal of Human Genetics|February 2, 2010
Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemiaLeana Doherty, Mee Rie Sheen, Adrianna Vlachos, et al.
American Journal of Human Genetics|December 9, 2008
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patientsHanna T Gazda, Mee Rie Sheen, Adrianna Vlachos, et al.
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