Cargando…

A novel cytogenetic abnormality t(7;8)(p11.2:q11.2) and a four-way Philadelphia translocation in an imatinib mesylate-resistant chronic myeloid leukemia patient

Chronic myelogenous leukemia (CML) is characterized by the Philadelphia (Ph) chromosome, created by a reciprocal translocation t(9:22)(q34;q11) which forms the chimeric gene, BCR-ABL. Variant Ph chromosome translocations involving chromosomes other than 9 and 22 have been identified in 5–10% of CML...

Descripción completa

Detalles Bibliográficos
Autores principales:	AL-ACHKAR, WALID, ALJAPAWE, ABDULMUNIM, ALMEDANI, SUHER, LIEHR, THOMAS, WAFA, ABDULSAMAD
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2013
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573104/ https://www.ncbi.nlm.nih.gov/pubmed/23420612 http://dx.doi.org/10.3892/ol.2012.1037

Ejemplares similares

Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patient
por: AL-ACHKAR, WALID, et al.
Publicado: (2013)

Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment
por: Wafa, Abdulsamad, et al.
Publicado: (2015)

A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case
por: AL-ACHKAR, WALID, et al.
Publicado: (2013)

Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient
por: AL-ACHKAR, WALID, et al.
Publicado: (2013)

An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations
por: AL-Achkar, Walid, et al.
Publicado: (2014)

Molecular Cytogenetic Characterization of an inv(Y)(p11.2q11.221∼q11.222) in a Syrian Family
por: Al-Achkar, W, et al.
Publicado: (2013)

Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report
por: Wafa, Abdulsamad, et al.
Publicado: (2016)

Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report
por: Wafa, Abdulsamad, et al.
Publicado: (2017)

De novo acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case report
por: ACHKAR, WALID AL, et al.
Publicado: (2014)

A novel dic (17;18) (p13.1;q11.2) with loss of TP53 and BCR/ABL rearrangement in an Imatinib resistant chronic myeloid leukemia
por: Al-achkar, Walid, et al.
Publicado: (2012)

A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia
por: Wafa, Abdulsamad, et al.
Publicado: (2016)

Xp11.2 Translocation Renal Cell Carcinoma Diagnosed by Immunohistochemistry and Cytogenetics
por: Dey, Biswajit, et al.
Publicado: (2016)

Acquired del(9)(p22.3) in a primary plasma cell leukemia
por: Achkar, Walid Al, et al.
Publicado: (2013)

Do novo del(9)(p13) in a childhood T-cell prolymphocytic leukemia as sole abnormality
por: Wafa, Abdulsamad, et al.
Publicado: (2014)

Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case
por: Al-Achkar, Walid, et al.
Publicado: (2011)

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, et al.
Publicado: (2018)

Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report
por: Al Achkar, Walid, et al.
Publicado: (2009)

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, et al.
Publicado: (2020)

A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints
por: Al-achkar, Walid, et al.
Publicado: (2013)

Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event
por: Wafa, Abdulsamad, et al.
Publicado: (2015)

A chronic myeloid leukemia case with a variant translocation t(11;22) (q23;q11.2): masked Philadelphia or simple variant translocation?
por: Acar, Kadir, et al.
Publicado: (2018)

Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family
por: Wafa, Abdulsamad, et al.
Publicado: (2022)

Clinicopathological features of Xp11.2 translocation renal cell carcinoma
por: Lim, Bumjin, et al.
Publicado: (2015)

Xp11.2 translocation renal cell carcinomas in young adults
por: Xu, Linfeng, et al.
Publicado: (2015)

Sensory processing in 16p11.2 deletion and 16p11.2 duplication
por: Smith, Harriet, et al.
Publicado: (2022)

Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male
por: Wiland, Ewa, et al.
Publicado: (2014)

Prenatal Diagnosis of a New Case: De Novo Balanced Non-Robertsonian Translocation Involving t(15;22)(p11.2;q11.2)
por: Atli, Eİ, et al.
Publicado: (2018)

Association between chromosome 22q11.2 translocation and male oligozoospermia
por: Zhan, Peng, et al.
Publicado: (2022)

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families
por: HUANG, LINHUAN, et al.
Publicado: (2015)

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2
por: Li, Meihua, et al.
Publicado: (2022)

Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits
por: Vysotskiy, Mikhail, et al.
Publicado: (2023)

Bilateral Xp11.2 translocation renal cell carcinoma: a case report
por: Karashima, Takashi, et al.
Publicado: (2018)

Estrogen associates with female predominance in Xp11.2 translocation renal cell carcinoma
por: Lu, Yanwen, et al.
Publicado: (2023)

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022)

Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
por: Kmetec, Andrej, et al.
Publicado: (2014)

Xp11.2 Translocation Renal Cell Carcinoma: Clinical Characteristics and Potential Prognostic Predictors
por: Dong, Jie, et al.
Publicado: (2021)

Xp11.2 Translocation Renal Cell Carcinoma: A Rare Renal Cell Carcinoma
por: Kalita, Pranjal, et al.
Publicado: (2023)

Case Report: Balanced Reciprocal Translocation t (17; 22) (p11.2; q11.2) and 10q23.31 Microduplication in an Infertile Male Patient Suffering From Teratozoospermia
por: Huang, Shan, et al.
Publicado: (2022)

Reciprocal Deletion and Duplication of 17p11.2-11.2: Korean Patients with Smith-Magenis Syndrome and Potocki-Lupski Syndrome
por: Lee, Cha Gon, et al.
Publicado: (2012)

Three patients with 46,X,inv(Y)(p11.2q11.2)pat/45,X and their pedigree analysis
por: Chen, Yunchun, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_7l2410t4j5r5db7vph9ji06ms6