Cargando…
Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants
BACKGROUND: De novo variants are a common cause to rare intellectual disability syndromes, associated with low recurrence risk. However, when such variants occur pre‐zygotically in parental germ cells, the recurrence risk might be higher. Still, the recurrence risk estimates are mainly based on empi...
Autores principales: | Frisk, Sofia, Wachtmeister, Alexandra, Laurell, Tobias, Lindstrand, Anna, Jäntti, Nina, Malmgren, Helena, Lagerstedt‐Robinson, Kristina, Tesi, Bianca, Taylan, Fulya, Nordgren, Ann |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000944/ https://www.ncbi.nlm.nih.gov/pubmed/35118825 http://dx.doi.org/10.1002/mgg3.1880 |
Ejemplares similares
-
Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth
por: Frisk, Sofia, et al.
Publicado: (2019) -
A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1
por: Pontén, Emeli, et al.
Publicado: (2022) -
Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes
por: Rahman, Muhammad M., et al.
Publicado: (2019) -
De novo diagnostics of patients with intellectual disability
por: Veltman, Joris A
Publicado: (2012) -
Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta
por: Andersson, Kristofer, et al.
Publicado: (2020)