Evaluation of loss of heterozygosity of chromosome 22q11.21 region in patients with congenital heart diseases

The 22q11.21 region is prone to low-copy repeats events that lead to congenital anomaly disorders. We tested genomic DNA of 20 families with non-syndromic CHD patients using a set of three known consecutive high polymorphic short tandem repeat (STR) markers along the 22q11.21 region; D22S941, D22S94...

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Detalles Bibliográficos
Autores principales: Behiry, Eman G., Abo Senna, Azza A., Elnagar, Amr E., Eshiesh, Magda A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Egyptian Society of Cardiology 2018
Materias:
Congenital Heart Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303538/
https://www.ncbi.nlm.nih.gov/pubmed/30591741
http://dx.doi.org/10.1016/j.ehj.2018.07.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303538/
https://www.ncbi.nlm.nih.gov/pubmed/30591741
http://dx.doi.org/10.1016/j.ehj.2018.07.003

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