Copy Number Changes in 1q21.3 and 1q23.3 have Different Clinical Relevance in Ovarian Tumors
Main Authors: | Dimova I, Orsetti B, Theillet Ch., Dimitrov R., Toncheva D |
---|---|
Format: | Article |
Language: | English |
Published: |
Sciendo
2009-01-01
|
Series: | Balkan Journal of Medical Genetics |
Subjects: | |
Online Access: | https://doi.org/10.2478/v10034-010-0009-5 |
Similar Items
-
Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene
by: Man Luo, et al.
Published: (2022-12-01) -
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
by: Gefei Xiao, et al.
Published: (2021-11-01) -
Prenatal diagnosis of a novel 7q31.31q31.33 microduplication with a favorable outcome
by: Huili Luo, et al.
Published: (2022-03-01) -
Unexplained Pancytopenia in a Patient with 5q35.2-q35.3 Microduplication Encompassing NSD1: A Case Report
by: Sungwoo Park, et al.
Published: (2018-10-01) -
Analysis of multiple chromosomal rearrangements in the genome of Willisornis vidua using BAC-FISH and chromosome painting on a supposed conserved karyotype
by: Talita Fernanda Augusto Ribas, et al.
Published: (2021-03-01)