Cargando…
A method of large DNA fragment enrichment for nanopore sequencing in region 22q11.2
Background: 22q11.2 deletion syndrome (22q11.2DS) is a disorder caused when a small part of chromosome 22 is missing. Diagnosis is currently established by the identification of a heterozygous deletion at chromosome 22q11.2 through chromosomal microarray analysis or other genomic analyses. However,...
Autores principales: | Lei, Yu-Qing, Xu, Liang-Pu, Cao, Hua, Wang, Xin-Rui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659874/ https://www.ncbi.nlm.nih.gov/pubmed/36386847 http://dx.doi.org/10.3389/fgene.2022.959883 |
Ejemplares similares
-
The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
por: Du, Qiumei, et al.
Publicado: (2020) -
The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS)()
por: van den Bree, Marianne B.M., et al.
Publicado: (2013) -
22q11.2 Low Copy Repeats Expanded in the Human Lineage
por: Vervoort, Lisanne, et al.
Publicado: (2021) -
miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome
por: Brzustowicz, Linda M., et al.
Publicado: (2012) -
Positive cfDNA screening results for 22q11.2 deletion syndrome—Clinical and laboratory considerations
por: Soster, Erica, et al.
Publicado: (2023)