Cargando…

Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study

The constitutional t(11;22)(q23;q11) translocation is the only recurrent non‐Robertsonian translocation known in humans. Carriers are phenotypically normal and are usually referred for cytogenetic testing because of multiple miscarriages, infertility, or having aneuploidy in offspring. A breast canc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Schoemaker, Minouk J, Jones, Michael E, Higgins, Craig D, Wright, Alan F, Swerdlow, Anthony J
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2019
Materias:	Cancer Epidemiology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767470/ https://www.ncbi.nlm.nih.gov/pubmed/30496607 http://dx.doi.org/10.1002/ijc.32031

Ejemplares similares

Intravascular Large B-cell Lymphoma of the Bilateral Ovaries and Uterus in an Asymptomatic Patient with a t(11;22)(q23;q11) Constitutional Translocation
por: Shigematsu, Yasuyuki, et al.
Publicado: (2016)

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)

MLL-SEPT5 Fusion Transcript in Myelodysplastic Syndrome Patient With t(11;22)(q23;q11)
por: Zou, Duobing, et al.
Publicado: (2021)

MLL-SEPT5 Fusion Transcript in Two de novo Acute Myeloid Leukemia Patients With t(11;22)(q23;q11)
por: Wang, Nana, et al.
Publicado: (2016)

Interstitial duplication of 20q11.22q13.11: A case report and review of literature
por: Goetzinger, Logan, et al.
Publicado: (2021)

Mortality and Cancer Incidence in Carriers of Balanced Robertsonian Translocations: A National Cohort Study
por: Schoemaker, Minouk J, et al.
Publicado: (2019)

A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome
por: Pastor, Steven, et al.
Publicado: (2022)

Clinical Characterization of a 6-Year-Old Patient with Autism and Two Adjacent Duplications on 10q11.22q11.23. A Case Report
por: Tritto, Giovanna, et al.
Publicado: (2021)

Detection of t(11;22)(q24;q12) translocation of Ewing's sarcoma in paraffin embedded tissue by nested reverse transcription-polymerase chain reaction.
por: Park, Y. K., et al.
Publicado: (1998)

Frequency of Translocation t(11;22)(q24;q12) Using Fluorescence In Situ Hybridization (FISH) in Histologically and Immunohistochemically Diagnosed Cases of Ewing’s Sarcoma
por: Bashir, Muhammad Rizwan, et al.
Publicado: (2020)

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation
por: Mishra, Divya, et al.
Publicado: (2014)

Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a de Novo 22q11.1q11.22 Duplication
por: Vaisvilas, M, et al.
Publicado: (2018)

Breast cancer risk in relation to history of preeclampsia and hyperemesis gravidarum: Prospective analysis in the Generations Study
por: Wright, Lauren B., et al.
Publicado: (2018)

Mixed lineage leukemia-septin 5 fusion transcript in de novo adult acute myeloid leukemia with t(11;22)(q23;q11.2): A case report
por: GAO, WEN, et al.
Publicado: (2014)

Establishment and Characterization of a Small Round Cell Sarcoma Cell Line, SCCH‐196, with t(11;22)(q24;q12)
por: Homma, Chieko, et al.
Publicado: (1989)

Rare Gene Rearrangement t(11;22)(q23;q13)/KMT2A-EP300 in Therapy-related Acute Myeloid Leukemia: A Case Report
por: Kim, Seo Wan, et al.
Publicado: (2022)

Risk of breast cancer in men in relation to weight change: A national case‐control study in England and Wales
por: Swerdlow, Anthony J., et al.
Publicado: (2022)

A low‐grade astrocytoma in a sixteen‐year‐old boy with a 7q11.22 deletion
por: van Kampen, Francoise S., et al.
Publicado: (2017)

A New Three-Way Translocation t(4;11;7)(q21;q23;q22) in a Mixed-Phenotype Acute Leukemia
por: Takasaki, Hirotaka, et al.
Publicado: (2011)

New Complex Chromosomal Translocation in Chronic Myeloid Leukaemia: t(9;18;22)(q34;p11;q11)
por: El Andaloussi, Abdeljabar, et al.
Publicado: (2007)

Genome‐wide association study identifies 7q11.22 and 7q36.3 associated with noise‐induced hearing loss among Chinese population
por: Niu, Yuguang, et al.
Publicado: (2020)

Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion
por: Gudbrandsen, Maria, et al.
Publicado: (2020)

Variant Burkitt-type translocation (8;22)(q24;q11) in plasma cell myeloma
por: Kim, Hanah, et al.
Publicado: (2011)

A case of chronic myelogenous leukemia in pregnancy characterized by a complex translocation t(9;22;11)(q34;q11.2;q13)
por: Kumar, Surachit, et al.
Publicado: (2011)

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

B-cell Acute Lymphoblastic Leukemia With t(9;22)(q34;q11) Translocation and Clonal Divergence Through ider(22) Chromosome and t(13;17)(q14;q25) Translocation
por: Meza-Espinoza, Juan Pablo, et al.
Publicado: (2016)

Prenatal cfDNA Screening for Emanuel Syndrome and Other Unbalanced Products of Conception in Carriers of the Recurrent Balanced Translocation t(11;22): One Laboratory’s Retrospective Experience
por: Soster, Erica, et al.
Publicado: (2023)

Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)
por: Chen, Rongyu, et al.
Publicado: (2014)

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)

Derivative 11;22 (Emanuel) Syndrome: A Case Report and A Review
por: Choudhary, Madan Gopal, et al.
Publicado: (2013)

Characterization of a de Novo Constitutional Balanced Translocation t (2;11)(q33.2;q23.2) with Break Point on the Human NBEAL1-GeneHo
por: KARIMZADHAGH, Javad, et al.
Publicado: (2018)

A novel five-way translocation t(7;11;9;22;9)(q22;q13;q34;q11.2;q34) involving Ph chromosome in a patient of chronic myeloid leukemia: a case report
por: Yokota, Sho, et al.
Publicado: (2012)

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
por: Hamdi, Yosr, et al.
Publicado: (2016)

Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019)

Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cord
por: Mascelli, Samantha, et al.
Publicado: (2014)

Are submicroscopic chromosomal inversions predisposing factors for the t(9;22)(q34;q11.2) translocation in chronic myeloid leukemia?
por: González García, Juan Ramón, et al.
Publicado: (2015)

The rare translocation t(14;21)(q11;q22) detected in a Moroccan patient with T-cell acute lymphoblastic leukemia
por: Chebihi, Z. Takki, et al.
Publicado: (2018)

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
por: Ghorbanoghli, Z., et al.
Publicado: (2016)

Prenatally detected six duplications at Xp22.33-p11.22: a case report
por: Zhang, Xue, et al.
Publicado: (2023)

The Danish 22q11 research initiative
por: Schmock, Henriette, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_1bepg3fuahmhosv04637pniee7