DiGeorge综合征（又称22q11.2缺失综合征）是一种由染色体异常引起的遗传性疾病。它涉及到22号染色体的微缺失，导致患者在多个系统中出现不同的 ...

An underlying genetic syndrome, most commonly trisomy 21 and DiGeorge syndrome, was present in 17 patients (30%). Among 28 patients (50%), PVS was the primary cardiac diagnosis in the context of ...

Children with congenital heart defects (CHD) have a significantly higher risk of mortality within five years following a cancer diagnosis compared to those without CHD. This risk is particularly ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate cardiac development ... Center at Houston DiGeorge syndrome, a 22q11.2 ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate cardiac development ... co-first author. DiGeorge syndrome, a 22q11.2 ...

A new bridge built as part of a project to widen a section of the A1 has been found to have defects. The Allerdene Bridge, in Gateshead, was replaced by a new structure that opened in September ...

SpectX, TNO, and partners GE Vernova and LM Wind Power, will start a 2-years project to detect sub-surface defects in wind turbine blades by drone X-ray inspection. The findings will be integrated ...

Background The prevalence of congenital heart defects (CHD) in Down syndrome (DS) varies considerably across studies (from 16% to 84%). This study aimed to estimate the prevalence of CHD in people ...

This is the opposite of what happens in crystals, whose ordered structure facilitates their mathematical description, as well as the identification of those "defects," which practically control ...