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Human Molecular Genetics|September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.Platelets|February 8, 2022
Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesisOrna Steinberg-Shemer, Naama Orenstein, Tanya Krasnov, et al.Haematologica|April 2, 2009
Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulatedSharon Noy-Lotan, Orly Dgany, Roxane Lahmi, et al.Journal of Pediatric Hematology/Oncology|June 4, 2016
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic AnalysisOrna Steinberg-Shemer, Siobán Keel, Orly Dgany, et al.European Journal of Haematology|February 5, 2017
Molecular diagnosis of α-thalassemia in a multiethnic populationOded Gilad, Orna Steinberg Shemer, Orly Dgany, et al.Clinical Genetics|December 19, 2024
A Variable Clinical Presentation of Hemoglobin City of HopeDafna Brik Simon, Dvora Filon, Vardiella Meiner, et al.British Journal of Haematology|December 28, 2020
Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopeniasSharon Noy-Lotan, Tanya Krasnov, Orly Dgany, et al.Pediatric Blood & Cancer|November 7, 2024
Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated NeutropeniaLital Oz-Alcalay, Orna Steinberg-Shemer, Eyal Elron, et al.British Journal of Haematology|August 16, 2005
Clinical and molecular variability in congenital dyserythropoietic anaemia type IHannah Tamary, Orly Dgany, Alexis Proust, et al.Pediatric Blood & Cancer|October 7, 2014
Genetic analysis and clinical picture of severe congenital neutropenia in IsraelAsaf Lebel, Joanne Yacobovich, Tanya Krasnov, et al.Pageof 5