Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications

• Glavni autori: Heine-Suñer Damià (Autor), Fibla Joan (Autor), Sánchez- (Autor), Rosell Jordi (Autor), Torres-Juan Laura (Autor)
• Format: Knjiga
• Izdano: BMC, 2007-04-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>The 22q11.2 deletion syndrome is the most frequent genomic disorder with an estimated frequency of 1/4000 live births. The majority of patients (90%) have the same deletion of 3 Mb (Typically Deleted Region, TDR) that results from ab...