Identification of a cryptic unbalanced translocation Der(22)t(12;22)(q24.33;q13.33) in a large Chinese family with Phelan-McDermid syndrome by nanopore sequencing
Abstract To explore the genetic cause of a four-generation severe intellectual disability in a Chinese family using nanopore sequencing and to provide genetic counseling and reproductive guidance for family members. Multiple genetic analyses of the proband and family members were performed, includin...
Saved in:
Main Authors: | Xingwu Wu, Qiang Xu, Ge Chen, Jialyv Huang, Yanying Zhong, Lifeng Tian, Qiongfang Wu, Jia Chen |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2025-01-01
|
Series: | Scientific Reports |
Subjects: | |
Online Access: | https://doi.org/10.1038/s41598-025-87083-8 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
An open-label study evaluating the safety and efficacy of AMO-01 for the treatment of seizures in Phelan-McDermid syndrome
by: Tess Levy, et al.
Published: (2025-04-01) -
9 Habilidades importantes de la comunicación para cada relación
by: Victor William Harris
Published: (2012-08-01) -
9 Habilidades importantes de la comunicación para cada relación
by: Victor William Harris
Published: (2012-08-01) -
Prenatal diagnosis of familial 2q13 microduplication and a de novo Xp22.33 microdeletion in a pregnancy associated with an asymptomatic mother carrier
by: Chih-Ping Chen
Published: (2025-01-01) -
8q22.2q22.3 Microdeletion Syndrome Associated with Hearing Loss and Intractable Epilepsy
by: Alejandra Rincon, et al.
Published: (2019-01-01)