Cargando…
Uniparental disomy in a population of 32,067 clinical exome trios
PURPOSE: Data on the clinical prevalence and spectrum of uniparental disomy (UPD) remain limited. Trio exome sequencing (ES) presents a comprehensive method for detection of UPD alongside sequence and copy-number variant analysis. METHODS: We analyzed 32,067 ES trios referred for diagnostic testing...
Autores principales: | Scuffins, Julie, Keller-Ramey, Jennifer, Dyer, Lindsay, Douglas, Ganka, Torene, Rebecca, Gainullin, Vladimir, Juusola, Jane, Meck, Jeanne, Retterer, Kyle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187148/ https://www.ncbi.nlm.nih.gov/pubmed/33495530 http://dx.doi.org/10.1038/s41436-020-01092-8 |
Ejemplares similares
-
Contribution of uniparental disomy in a clinical trio exome cohort of 2675 patients
por: Wang, Lei, et al.
Publicado: (2021) -
Accurate detection of clinically relevant uniparental disomy from exome sequencing data
por: Yauy, Kevin, et al.
Publicado: (2019) -
Cytogenetic contribution to uniparental disomy (UPD)
por: Liehr, Thomas
Publicado: (2010) -
Alström syndrome caused by maternal uniparental disomy
por: Lopour, Madeline Q.R., et al.
Publicado: (2022) -
Maternal Uniparental Disomy 14 (UPD14) Identified by Clinical Exome Sequencing in an Adolescent with Diverticulosis
por: Chan, Alvin P., et al.
Publicado: (2019)