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Fady M Mikhail

Showing results (11-20 of 74) with videos related to

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Cancer Research|September 6, 2005
The distal zinc finger domain of AML1/MDS1/EVI1 is an oligomerization domain involved in induction of hematopoietic differentiation defects in primary cells in vitroVitalyi Senyuk, Donglan Li, Alexander Zakharov, et al.
Clinical Case Reports|June 8, 2017
Concomitant imatinib and ibrutinib in a patient with chronic myelogenous leukemia and chronic lymphocytic leukemiaLauren K Shea, Fady M Mikhail, Andres Forero-Torres, et al.
Case Reports in Hematology|February 27, 2019
Relapse after Prolonged Remission in Philadelphia-Like Acute Lymphoblastic LeukemiaGaurav Shah, Fady M Mikhail, Andrew J Carroll, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|December 10, 2014
Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or PalateKitiwan Rojnueangnit, Fady M Mikhail, Xiangqin Cui, et al.
Oncogene|June 26, 2002
The leukemia-associated transcription repressor AML1/MDS1/EVI1 requires CtBP to induce abnormal growth and differentiation of murine hematopoietic cellsVitalyi Senyuk, Soumen Chakraborty, Fady M Mikhail, et al.
Genetic Testing and Molecular Biomarkers|June 26, 2010
Identification of PKHD1 multiexon deletions using multiplex ligation-dependent probe amplification and quantitative polymerase chain reactionVal Zvereff, Suxia Yao, Julia Ramsey, et al.
The Journal of Craniofacial Surgery|September 22, 2010
Use of array comparative genome hybridization in orofacial cleftingCarlos J Gallego, John Grant, Fady M Mikhail, et al.
Pediatric Neurology|September 13, 2011
Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopiaMaria Descartes, Fady M Mikhail, Judith C Franklin, et al.
The Journal of Pediatrics|September 10, 2014
Incidental detection of cancer predisposition gene copy number variations by array comparative genomic hybridizationJ Austin Hamm, Fady M Mikhail, Dana Hollenbeck, et al.
Clinical Case Reports|April 12, 2018
A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literatureJariya Upadia, Joseph B Philips, Nathaniel H Robin, et al.
Pageof 8

Showing results (11-20 of 74) with videos related to

Sort By:
Pageof 8
Cancer Research|September 6, 2005
The distal zinc finger domain of AML1/MDS1/EVI1 is an oligomerization domain involved in induction of hematopoietic differentiation defects in primary cells in vitroVitalyi Senyuk, Donglan Li, Alexander Zakharov, et al.
Clinical Case Reports|June 8, 2017
Concomitant imatinib and ibrutinib in a patient with chronic myelogenous leukemia and chronic lymphocytic leukemiaLauren K Shea, Fady M Mikhail, Andres Forero-Torres, et al.
Case Reports in Hematology|February 27, 2019
Relapse after Prolonged Remission in Philadelphia-Like Acute Lymphoblastic LeukemiaGaurav Shah, Fady M Mikhail, Andrew J Carroll, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|December 10, 2014
Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or PalateKitiwan Rojnueangnit, Fady M Mikhail, Xiangqin Cui, et al.
Oncogene|June 26, 2002
The leukemia-associated transcription repressor AML1/MDS1/EVI1 requires CtBP to induce abnormal growth and differentiation of murine hematopoietic cellsVitalyi Senyuk, Soumen Chakraborty, Fady M Mikhail, et al.
Genetic Testing and Molecular Biomarkers|June 26, 2010
Identification of PKHD1 multiexon deletions using multiplex ligation-dependent probe amplification and quantitative polymerase chain reactionVal Zvereff, Suxia Yao, Julia Ramsey, et al.
The Journal of Craniofacial Surgery|September 22, 2010
Use of array comparative genome hybridization in orofacial cleftingCarlos J Gallego, John Grant, Fady M Mikhail, et al.
Pediatric Neurology|September 13, 2011
Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopiaMaria Descartes, Fady M Mikhail, Judith C Franklin, et al.
The Journal of Pediatrics|September 10, 2014
Incidental detection of cancer predisposition gene copy number variations by array comparative genomic hybridizationJ Austin Hamm, Fady M Mikhail, Dana Hollenbeck, et al.
Clinical Case Reports|April 12, 2018
A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literatureJariya Upadia, Joseph B Philips, Nathaniel H Robin, et al.
Pageof 8