Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland

• Main Authors: Zeyland Joanna (Author), Krawczynski Maciej R (Author), Skolozdrzy Joanna (Author), Badura-Stronka Magdalena (Author), Moszura Tomasz (Author), Materna-Kiryluk Anna (Author), Glazar Renata (Author), Wisniewska Marzena (Author), Wolnik-Brzozowska Danuta (Author), Wozniak Anna (Author), Bobkowski Waldemar (Author), Slomski Ryszard (Author), Latos-Bielenska Anna (Author), Siwinska Aldona (Author)
• Format: Book
• Published: BMC, 2010-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>The 22q11.2 microdeletion syndrome (22q11.2 deletion syndrome -22q11.2DS) refers to congenital abnormalities, including primarily heart defects and facial dysmorphy, thymic hypoplasia, cleft palate and hypocalcaemia. Microdeletion wi...