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Harefuah|January 30, 2023
[GENETIC PANELS FOR THE DIAGNOSIS OF RARE CONGENITAL HEMATOLOGICAL DISORDERS]Orna Steinberg-Shemer, Orly Dgany, Hannah Tamary
Journal of Pediatric Hematology/Oncology|March 21, 2013
MPL Baltimore mutation and thrombocytosis: case report and literature reviewVered Shkalim-Zemer, Orly Dgany, Tanya Krasnov, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|August 10, 2007
Drosophila odz gene is required for multiple cell types in the compound retinaYael Kinel-Tahan, Hanna Weiss, Orly Dgany, et al.
The Israel Medical Association Journal : IMAJ|October 23, 2002
The molecular biology of Fanconi anemiaHannah Tamary, Raanan Bar-Yam, Michal Zemach, et al.
Journal of Pediatric Hematology/Oncology|November 16, 2004
A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type IHanna Shalev, Joseph Kapelushnik, Asher Moser, et al.
Journal of Pediatric Hematology/Oncology|October 9, 2012
From blood smear to lipid disorder: a case reportSarah Elitzur, Joanne Yacobovich, Orly Dgany, et al.
European Journal of Haematology|July 30, 2017
Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosisPeretz Resnitzky, Dina Shaft, Hanna Shalev, et al.
Acta Haematologica|January 15, 2020
Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So SilentOded Gilad, Orna Steinberg-Shemer, Orly Dgany, et al.
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