Coarctation of the aorta and mild to moderate developmental delay in a child with a <it>de novo </it>deletion of chromosome 15(q21.1q22.2)

• Auteurs principaux: Peters Sarika U (Auteur), Sanders Merideth E (Auteur), Sahoo Trilochan (Auteur), Lalani Seema R (Auteur), Bejjani Bassem A (Auteur)
• Format: Livre
• Publié: BMC, 2006-02-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Deletion of 15q21q22 is a rare chromosomal anomaly. To date, there have been nine reports describing ten individuals with different segmental losses involving 15q21 and 15q22. Many of these individuals have common features of growth...