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Harefuah|March 28, 2018
[EXOME ANALYSIS - A GAME CHANGER IN PEDIATRICS]Asaf Ta-Shma, Simon Edvardson, Orly Elpeleg, et al.Clinical Immunology (Orlando, Fla.)|March 4, 2014
Hematopoietic stem cell transplantation conditioning with use of rituximab in EBV related lymphoproliferative disordersOded Shamriz, Shoshana Revel Vilk, Dana G Wolf, et al.European Journal of Human Genetics : EJHG|August 3, 2017
Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemiaBassam Abu-Libdeh, Liza Douiev, Sarah Amro, et al.Journal of Medical Genetics|May 12, 2012
A human laterality disorder associated with recessive CCDC11 mutationZeev Perles, Yuval Cinnamon, Asaf Ta-Shma, et al.European Journal of Human Genetics : EJHG|December 4, 2014
A human laterality disorder associated with a homozygous WDR16 deletionAsaf Ta-Shma, Zeev Perles, Barak Yaacov, et al.American Journal of Medical Genetics. Part A|November 21, 2013
Isolated truncus arteriosus associated with a mutation in the plexin-D1 geneAsaf Ta-Shma, Ciro Leonardo Pierri, Polina Stepensky, et al.American Journal of Medical Genetics. Part A|February 7, 2020
Grandparental genotyping enhances exome variant interpretationHagit Daum, Hagar Mor-Shaked, Asaf Ta-Shma, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 14, 2007
Analysis of segmental and global function of the fetal heart using novel automatic functional imagingAsaf Ta-Shma, Zeev Perles, Sagui Gavri, et al.Annals of Neurology|August 30, 2016
Therapy with eculizumab for patients with CD59 p.Cys89Tyr mutationDror Mevorach, Inna Reiner, Amir Grau, et al.Journal of Medical Genetics|October 3, 2015
A human laterality disorder caused by a homozygous deleterious mutation in MMP21Zeev Perles, Sungjin Moon, Asaf Ta-Shma, et al.Pageof 3