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

• Asıl Yazarlar: Estivill Xavier (Yazar), Gabau Elisabeth (Yazar), García-Aragonés Manel (Yazar), Heine Damià (Yazar), Rosell Jordi (Yazar), Armengol Lluís (Yazar), Brunet Anna (Yazar), Guitart Miriam (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2009-12-01T00:00:00Z.
• Konular: article
• Online Erişim: 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>...