Cargando…
A Novel Four-Way Complex Variant Translocation Involving Chromosome 46,XY,t(4;9;19;22)(q25:q34;p13.3;q11.2) in a Chronic Myeloid Leukemia Patient
Philadelphia (Ph) chromosome (9;22)(q34;q11) is well established in more than 90% of chronic myeloid leukemia (CML) patients, and the remaining 5–8% of CML patients show variant and complex translocations, with the involvement of third, fourth, or fifth chromosome other than 9;22. However, in very r...
Autores principales: | Asif, Muhammad, Jamal, Mohammad Sarwar, Khan, Abdul Rehman, Naseer, Muhammad Imran, Hussain, Abrar, Choudhry, Hani, Malik, Arif, Khan, Shahida Aziz, Mahmoud, Maged Mostafa, Ali, Ashraf, Iram, Saima, Kamran, Kashif, Iqbal, Asim, Abduljaleel, Zainularifeen, Pushparaj, Peter Natesan, Rasool, Mahmood |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885335/ https://www.ncbi.nlm.nih.gov/pubmed/27303656 http://dx.doi.org/10.3389/fonc.2016.00124 |
Ejemplares similares
-
The psychiatric phenotype of 15q11.2-q13.3 duplications
por: Budisteanu, M., et al.
Publicado: (2021) -
Cytogenetical and hematological analysis of chronic myelogenous leukemia patients with a novel case 52XX, t (1;9;22) (q23.3; q34; q11.2), +6, +8, i(9) (q10;q10), +18,+19,+21+der22 t(9;22)(q34;q11)
por: Asif, Muhammad, et al.
Publicado: (2022) -
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders
por: Isles, Anthony R., et al.
Publicado: (2016) -
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
por: Manolakos, Emmanouil, et al.
Publicado: (2011) -
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
por: Manolakos, Emmanouil, et al.
Publicado: (2011)