Exclusion of chromosomal abnormalities and microdeletions 22q11 and 10p13 in Algerian patients with isolated conotruncal malformation

• Published in: Цитология и генетика
• Date: 2015
• Main Authors: Ammar-Khodja, F., Abdellali, M.
• Format: Article
• Language: English
• Published: Інститут клітинної біології та генетичної інженерії НАН України 2015
• Subjects: Оригинальные работы
• Online Access: https://nasplib.isofts.kiev.ua/handle/123456789/126702
• Journal Title: Digital Library of Periodicals of National Academy of Sciences of Ukraine
• Cite this: Exclusion of chromosomal abnormalities and microdeletions 22q11 and 10p13 in Algerian patients with isolated conotruncal malformation / F. Ammar-Khodja, M. Abdellali // Цитология и генетика. — 2015. — Т. 49, № 1. — С. 45-51. — Бібліогр.: 50 назв. — англ.

The chromosomal abnormalities of number and structure or the 22q11.2 and 10p13-14 microdeletions are considered the main causes of congenital heart disease. In our best knowledge, cytogenetics studies on congenital heart diseases (CHD) have not been performed in Algeria. In this study, we will scree...