Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15.
We describe a stromal predominant Wilms tumor with focal anaplasia and a complex, tumor specific chromosome 11 aberration: a homozygous deletion of the entire WT1 gene within a heterozygous 11p13 deletion and an additional region of uniparental disomy (UPD) limited to 11p15.5-p15.2 including the IGF...
Saved in:
| Main Authors: | Artur Brandt, Katharina Löhers, Manfred Beier, Barbara Leube, Carmen de Torres, Jaume Mora, Parineeta Arora, Parmjit S Jat, Brigitte Royer-Pokora |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2016-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0155561&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Neuropathology of 16p13.11 deletion in epilepsy.
by: Joan Y W Liu, et al.
Published: (2012-01-01) -
Hyperinsulinemic Hypoglycemia and Growth Hormone Deficiency Secondary to 20p11 Deletion
by: Erica Wee, et al.
Published: (2023-01-01) -
P394: Case study of Yp11.31 deletion in XXY phenotypic female
by: Megan Wassef, et al.
Published: (2025-01-01) -
27: Siblings with reciprocal duplication/ deletions of 11p and 20p due to segregation of complex chromosomal rearrangements
by: Sarah Beaudry, et al.
Published: (2025-01-01) -
Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion
by: Jente Verbesselt, et al.
Published: (2025-06-01)