Cargando…
Cytogenetically visible inversions are formed by multiple molecular mechanisms
Cytogenetically detected inversions are generally assumed to be copy number and phenotypically neutral events. While nonallelic homologous recombination is thought to play a major role, recent data suggest the involvement of other molecular mechanisms in inversion formation. Using a combination of s...
Autores principales: | Pettersson, Maria, Grochowski, Christopher M., Wincent, Josephine, Eisfeldt, Jesper, Breman, Amy M., Cheung, Sau W., Krepischi, Ana C. V., Rosenberg, Carla, Lupski, James R., Ottosson, Jesper, Lovmar, Lovisa, Gacic, Jelena, Lundberg, Elisabeth S., Nilsson, Daniel, Carvalho, Claudia M. B., Lindstrand, Anna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702065/ https://www.ncbi.nlm.nih.gov/pubmed/32906200 http://dx.doi.org/10.1002/humu.24106 |
Ejemplares similares
-
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
por: Nazaryan-Petersen, Lusine, et al.
Publicado: (2018) -
Chromoanagenesis Event Underlies a de novo Pericentric and Multiple Paracentric Inversions in a Single Chromosome Causing Coffin–Siris Syndrome
por: Grochowski, Christopher M., et al.
Publicado: (2021) -
Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements
por: Eisfeldt, Jesper, et al.
Publicado: (2019) -
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier
por: Eisfeldt, Jesper, et al.
Publicado: (2020) -
AMYCNE: Confident copy number assessment using whole genome sequencing data
por: Eisfeldt, Jesper, et al.
Publicado: (2018)