Complex rearrangement in acute myeloid leukemia M2 with RUNX1/RUNX1T1 fusion involving chromosomes 8, 17 and 21

por Mishra, Shiba Ranjan, Rawal, Leena, Othman, Moneeb A. K., Thatai, Atul, Sarkar, Aditi, Lal, Vandana, Bhattacharya, Saurabh Kumar
Publicado 2021

A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML

por Wafa, Abdulsamad, ALmedania, Suher, Aljapawe, Abdulmunim, Liehr, Thomas, Soulaiman, Soulaiman E., Mouna, Raja, Othman, Moneeb A. K., ALachkar, Walid
Publicado 2018

A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia

por Othman, Moneeb A. K., Rincic, Martina, Melo, Joana B., Carreira, Isabel M., Alhourani, Eyad, Hunstig, Friederike, Glaser, Anita, Liehr, Thomas
Publicado 2014

Molecular cytogenetic pilot study on pleomorphic adenomas of salivary glands

por Thielker, Jovanna, Weise, Anja, Othman, Moneeb A.K., Carreria, Isabel M., Melo, Joana B., Von Eggeling, Ferdinand, Guntinas-Lichius, Orlando, Ziegler, Monika, Liehr, Thomas
Publicado 2020

An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case

por Wafa, Abdulsamad, Jarjour, Rami A., Aljapawe, Abdulmunim, ALmedania, Suher, Liehr, Thomas, Melo, Joana B., Carreira, Isabel M., Othman, Moneeb A. K., Al-Achkar, Walid
Publicado 2020

A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome

por Wafa, Abdulsamad, Jarjour, Rami A., Alolabi, Doaa, Liehr, Thomas, Hamdan, Othman, Melo, Joana B., Carreira, Isabel M., Othman, Moneeb A. K., Al-Achkar, Walid
Publicado 2020

BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients

por ALHOURANI, EYAD, OTHMAN, MONEEB A.K., MELO, JOANA B., CARREIRA, ISABEL M., GRYGALEWICZ, BEATA, VUJIĆ, DRAGANA, ZECEVIĆ, ZELJKO, JOKSIĆ, GORDANA, GLASER, ANITA, POHLE, BEATE, SCHLIE, CORDULA, HAUKE, SVEN, LIEHR, THOMAS
Publicado 2016

Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia

por de Figueiredo, Amanda Faria, Capela de Matos, Roberto Rodrigues, Othman, Moneeb A. K., Liehr, Thomas, da Costa, Elaine Sobral, Land, Marcelo Geradin Poirot, Ribeiro, Raul C., Abdelhay, Eliana, Silva, Maria Luiza Macedo
Publicado 2015

A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome

por de Souza, Daiane Correa, de Figueiredo, Amanda Faria, Ney Garcia, Daniela R., da Costa, Elaine Sobral, Othman, Moneeb A.K., Liehr, Thomas, Abdelhay, Eliana, Silva, Maria Luiza Macedo, de Souza Fernandez, Teresa
Publicado 2017

High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia

por Othman, Moneeb A. K., Melo, Joana B., Carreira, Isabel M., Rincic, Martina, Glaser, Anita, Grygalewicz, Beata, Gruhn, Bernd, Wilhelm, Kathleen, Rittscher, Katharina, Meyer, Britta, Silva, Maria Luiza Macedo, de Jesus Marques Salles, Terezinha, Liehr, Thomas
Publicado 2015

Parental origin of deletions and duplications – about the necessity to check for cryptic inversions

por Liehr, Thomas, Schreyer, Isolde, Kuechler, Alma, Manolakos, Emmanouil, Singer, Sylke, Dufke, Andreas, Wilhelm, Kathleen, Jančušková, Tereza, Čmejla, Radek, Othman, Moneeb A. K., Al-Rikabi, Ahmed H., Mrasek, Kristin, Ziegler, Monika, Kankel, Stefanie, Kreskowski, Katharina, Weise, Anja
Publicado 2018