Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period
The prenatal diagnosis of congenital heart disease (CHD) is important because of mortality risk. The onset of CHD varies, and depending on the malformation type, the risk of aneuploidy is changed. To identify possible genetic alterations in CHD, G-banding, chromosomal microarray or if needed DNA mut...
Guardado en:
Autores principales: | Emine Ikbal Atli, Engin Atli, Sinem Yalcintepe, Selma Demir, Rasime Kalkan, Cisem Akurut, Yasemin Ozen, Hakan Gurkan |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Georg Thieme Verlag KG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/394510a10a014c37a951580b9a283724 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
A Pilot Study about Clinical Features of Aberrations Chromosome 22q
por: Emine Ikbal Atli, et al.
Publicado: (2021) -
Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants
por: Selma Demir, et al.
Publicado: (2021) -
Pulse oximetry screening: a review of diagnosing critical congenital heart disease in newborns
por: Engel MS, et al.
Publicado: (2016) -
Maternal sociodemographic characteristics, early pregnancy behaviours, and livebirth outcomes as congenital heart defects risk factors - Northern Ireland 2010-2014
por: Hafi Saad, et al.
Publicado: (2021) -
Congenital heart disease
Publicado: (2006)