Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)
Objective: Congenital diaphragmatic hernia (CDH) is a congenital birth defect affecting around 1/3000 births. We propose that a significant number of isolated CDH cases have an underlying genetic cause, and that a subset of these result from copy number variations (CNVs) identifiable by array CGH. M...
Saved in:
Main Authors: | Kasemsri Srisupundit, Paul D. Brady, Koenraad Devriendt, Jean Pierre Fryns, Rogelio Cruz-Martinez, Eduard Gratacos, Jan A. Deprest, Joris R. Vermeesch |
---|---|
格式: | 雜誌 |
出版: |
2018
|
主題: | |
在線閱讀: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78649655581&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51024 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
相似書籍
-
Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)
由: Srisupundit K., et al.
出版: (2014) -
Recent developments in the genetic factors underlying congenital diaphragmatic hernia
由: Paul D. Brady, et al.
出版: (2018) -
Recent developments in the genetic factors underlying congenital diaphragmatic hernia
由: Brady P., et al.
出版: (2017) -
Classification of array CGH data using smoothed logistic regression model
由: Huang, J., et al.
出版: (2011) -
Successful management of Congenital Diaphragmatic Hernia (CDH) in an 8-day-old infant with moderate persistent pulmonary hypertension, moderate muscular Ventricular Septal Defect (VSD), and small Patent Ductus Arteriosus (PDA).
由: Oktavian Prasetia Wardana, -, et al.