BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1

• Main Authors: Estivill Xavier (Author), Gabau Elisabeth (Author), García-Aragonés Manel (Author), Heine Damià (Author), Rosell Jordi (Author), Armengol Lluís (Author), Brunet Anna (Author), Guitart Miriam (Author)
• Format: Knjiga
• Izdano: BMC, 2009-12-01T00:00:00Z.
• Teme: article
• Online dostop: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Microdeletion of the chromosome 22q11.2 region is the most common genetic aberration among patients with velocardiofacial syndrome (VCFS) but a subset of subjects do not show alterations of this chromosome region.</p> <p>...