BCR-JAK2 fusion as a result of a translocation (9;22)(p24;q11.2) in a patient with CML-like myeloproliferative disease

por Elnaggar, Mohamed M, Agersborg, Sally, Sahoo, Trilochan, Girgin, Ati, Ma, Wanlong, Rakkhit, Ronjay, Zorrilla, Isabel, Leal, Alexis
Publicado 2012

CMA analysis identifies homozygous deletion of MCPH1 in 2 brothers with primary Microcephaly-1

por Hemmat, Morteza, Rumple, Melissa J, Mahon, Loretta W, Morrow, Melanie, Zach, Tamara, Anguiano, Arturo, Elnaggar, Mohamed M, Wang, Boris T, Boyar, Fatih Z
Publicado 2017

Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay

por Hemmat, Morteza, Yang, Xiaojing, Chan, Patricia, McGough, Robert A, Ross, Leslie, Mahon, Loretta W, Anguiano, Arturo L, Boris, Wang T, Elnaggar, Mohamed M, Wang, Jia-Chi J, Strom, Charles M, Boyar, Fatih Z
Publicado 2014