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Mohamed M Elnaggar
Mohamed M Elnaggar
Quest Diagnostics
Genetics
Biology
Human genetics
Chromosome
Cytogenetics
5
Papers
57
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CMA Analysis Identifies Homozygous Deletion of MCPH1 in 2 Brothers with Primary Microcephaly-1
2017
Molecular Cytogenetics
Morteza Hemmat
Melissa Rumple
Loretta W Mahon
Melanie Morrow
Tamara Zach
Arturo Anguiano
Mohamed M Elnaggar
Boris T Wang
Fatih Z Boyar
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Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements
2015
European Journal of Human Genetics
Trilochan Sahoo
Jia-Chi Wang
Mohamed M Elnaggar
Pedro A. Sanchez-Lara
Leslie Ross
Loretta W Mahon
Katayoun Hafezi
Abigail Deming
Lynne Hinman
Yovana Bruno
James A Bartley
Thomas Liehr
Arturo Anguiano
Marilyn C. Jones
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Citations (18)
Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay
2014
Molecular Cytogenetics
Morteza Hemmat
Xiaojing Yang
Patricia Chan
Robert A McGough
Leslie Ross
Loretta W Mahon
Arturo Anguiano
Wang T Boris
Mohamed M Elnaggar
Jia-Chi J Wang
Charles M. Strom
Fatih Z Boyar
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Citations (3)
Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory
2014
Molecular Cytogenetics
Boris T Wang
Thomas P Chong
Fatih Z Boyar
Kimberly A Kopita
Leslie Ross
Mohamed M Elnaggar
Trilochan Sahoo
Jia-Chi Wang
Morteza Hemmat
Mary Haddadin
Renius Owen
Arturo Anguiano
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Citations (24)
BCR-JAK2 fusion as a result of a translocation (9;22)(p24;q11.2) in a patient with CML-like myeloproliferative disease
2012
Molecular Cytogenetics
Mohamed M Elnaggar
Sally Agersborg
Trilochan Sahoo
Ati Girgin
Wanlong Ma
Ronjay Rakkhit
Isabel Zorrilla
Alexis Leal
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Citations (12)
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