Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Moneeb Abdullah Kassem Othman"'
Autor:
Liena Elbaghir Omer Elsayed, Norah Ayed AlHarbi, Ashwaq Mohammed Alqarni, Huda Hussein Elwasila Eltayeb, Noura Mostafa Mohamed Mostafa, Maha Mohammed Abdulrahim, Hadeel Ibrahim Bin Zaid, Latifah Mansour Alanzi, Sarah Abdullah Ababtain, Khawlah Aldulaijan, Sheka Yagub Aloyouni, Moneeb Abdullah Kassem Othman, Mohammad Abdullah Alkheilewi, Adel Mohammed Binduraihem, Hadeel Abdollah Alrukban, Hiba Yousif Ahmed, Faten Abdullah AlRadini, Hadil Mohammad Alahdal, Aziza Mufareh Mushiba, Omaima Abdulazeem Alzaher
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-10 (2024)
Abstract Background Chromosome 16p11.2 deletions and duplications were found to be the second most common copy number variation (CNV) reported in cases with clinical presentation suggestive of chromosomal syndromes. Chromosome 16p11.2 deletion syndro
Externí odkaz:
https://doaj.org/article/c35507dced82439484a71711a4834fd0
Autor:
Abdulsamad Wafa, Walid Al Achkar, Abdulmunim Aljapawe, Thomas Liehr, Moneeb Abdullah Kassem Othman
Publikováno v:
Case Reports in Clinical Medicine. :517-520
The so-calledPhiladelphia(Ph) chromosome is present in more than 90% of chronic myeloid leukemia (CML) cases. It results in juxtaposition of the 5' part of the BCR gene on chromosome 22 and the 3' part of the ABL1 gene on chromosome 9. An additional
Publikováno v:
Molecular Cytogenetics
Background: Acute myelogeneous leukemia (AML) is a malignancy of the hematopoietic stem cells, for which cytogenetic analysis is still one of the most important diagnostic and prognostic tools. Still, we are far away from having seen and described al
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 5, Iss 1, p 36 (2012)
Molecular Cytogenetics, Vol 5, Iss 1, p 36 (2012)
Background The so-called Philadelphia (Ph) chromosome is present in more than 90% of chronic myeloid leukemia (CML) cases. It results in juxtaposition of the 5′ part of the BCR gene on chromosome 22 to the 3′ part of the ABL gene on chromosome 9.
Autor:
AL-Achkar, Walid, Wafa, Abdulsamad, Moneeb Abdullah Kassem Othman, Moassass, Faten, Aljapawe, Abdulmunim, Liehr, Thomas
Publikováno v:
Molecular Cytogenetics (17558166); 2014, Vol. 7 Issue 1, p1-10, 10p
Autor:
Walid Al-Achkar, Abdulsamad Wafa, Abdulmunim Aljapawe, Moneeb Abdullah Kassem Othman, Thomas Liehr, Faten Moassass
Publikováno v:
Molecular Cytogenetics
Background: We report a clinically diagnosed acute lymphoblastic leukemia (ALL) with yet unreported secondary chromosomal aberrations. Results: A complete cytogenetic and molecular cytogenetic analysis, using GTG banding, fluorescence in situ hybridi