Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Fady M Mikhail

Showing results (61-70 of 74) with videos related to

Pageof 8
Sort By:
The American Journal of Pathology|January 17, 2013
Transgenic mice overexpressing neuregulin-1 model neurofibroma-malignant peripheral nerve sheath tumor progression and implicate specific chromosomal copy number variations in tumorigenesisSyed J Kazmi, Stephanie J Byer, Jenell M Eckert, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)Fady M Mikhail, Achara Sathienkijkanchai, Nathaniel H Robin, et al.
British Journal of Haematology|February 16, 2026
Validation of the 2025 IMS/IMWG risk classification in patients with newly diagnosed multiple myeloma treated with quadruplets and autologous stem cell transplantPriyanka Venkatesh, Gayathri Ravi, Binod Dhakal, et al.
Genes, Chromosomes & Cancer|August 7, 2023
Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndromePatrick R Blackburn, Rose B McGee, Roya Mostafavi, et al.
Cancer Genetics|April 18, 2020
Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemiaYassmine M N Akkari, Helene Bruyere, R Tanner Hagelstrom, et al.
Leukemia & Lymphoma|July 26, 2023
Utility of end of induction bone marrow biopsy and survival outcomes in acute promyelocytic leukemia treated with fixed-dose induction regimenSydney Dunn-Valadez, Srilakshmi Bathini, Kathleen E Purdy, et al.
Clinical Genetics|July 26, 2023
Inherited CSNK2A1 variants in families with Okur-Chung neurodevelopmental syndromeNewell Belnap, Aiai Price-Smith, Keri Ramsey, et al.
Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.
Blood|February 9, 2010
Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemiaRichard C Harvey, Charles G Mullighan, I-Ming Chen, et al.
Cancer Causes & Control : CCC|November 25, 2015
Family history of hematologic malignancies and risk of multiple myeloma: differences by race and clinical featuresMaryAnn E VanValkenburg, Gwendolyn I Pruitt, Ilene K Brill, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
The American Journal of Pathology|January 17, 2013
Transgenic mice overexpressing neuregulin-1 model neurofibroma-malignant peripheral nerve sheath tumor progression and implicate specific chromosomal copy number variations in tumorigenesisSyed J Kazmi, Stephanie J Byer, Jenell M Eckert, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)Fady M Mikhail, Achara Sathienkijkanchai, Nathaniel H Robin, et al.
British Journal of Haematology|February 16, 2026
Validation of the 2025 IMS/IMWG risk classification in patients with newly diagnosed multiple myeloma treated with quadruplets and autologous stem cell transplantPriyanka Venkatesh, Gayathri Ravi, Binod Dhakal, et al.
Genes, Chromosomes & Cancer|August 7, 2023
Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndromePatrick R Blackburn, Rose B McGee, Roya Mostafavi, et al.
Cancer Genetics|April 18, 2020
Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemiaYassmine M N Akkari, Helene Bruyere, R Tanner Hagelstrom, et al.
Leukemia & Lymphoma|July 26, 2023
Utility of end of induction bone marrow biopsy and survival outcomes in acute promyelocytic leukemia treated with fixed-dose induction regimenSydney Dunn-Valadez, Srilakshmi Bathini, Kathleen E Purdy, et al.
Clinical Genetics|July 26, 2023
Inherited CSNK2A1 variants in families with Okur-Chung neurodevelopmental syndromeNewell Belnap, Aiai Price-Smith, Keri Ramsey, et al.
Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.
Blood|February 9, 2010
Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemiaRichard C Harvey, Charles G Mullighan, I-Ming Chen, et al.
Cancer Causes & Control : CCC|November 25, 2015
Family history of hematologic malignancies and risk of multiple myeloma: differences by race and clinical featuresMaryAnn E VanValkenburg, Gwendolyn I Pruitt, Ilene K Brill, et al.
Pageof 8