Cargando…
Cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangement
BACKGROUND: Precise characterization of apparently balanced complex chromosomal rearrangements in non-affected individuals is crucial as they may result in reproductive failure, recurrent miscarriages or affected offspring. CASE PRESENTATION: We present a family, where the non-affected father and da...
Autores principales: | Aristidou, Constantia, Theodosiou, Athina, Ketoni, Andria, Bak, Mads, Mehrjouy, Mana M., Tommerup, Niels, Sismani, Carolina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991433/ https://www.ncbi.nlm.nih.gov/pubmed/29930709 http://dx.doi.org/10.1186/s13039-018-0384-2 |
Ejemplares similares
-
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing
por: Aristidou, Constantia, et al.
Publicado: (2017) -
Position effect, cryptic complexity, and direct gene disruption as disease mechanisms in de novo apparently balanced translocation cases
por: Aristidou, Constantia, et al.
Publicado: (2018) -
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing
por: Aristidou, Constantia, et al.
Publicado: (2022) -
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2
por: Nazaryan, Lusine, et al.
Publicado: (2014) -
Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes
por: Luukkonen, Tiia Maria, et al.
Publicado: (2017)