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)

by Peters Sarika U, Sanders Merideth E, Sahoo Trilochan, Lalani Seema R, Bejjani Bassem A
Published 2006-02-01

SNP genotyping to screen for a common deletion in CHARGE Syndrome

by Molinari Laura M, Bacino Carlos A, Phillips Michael, Fernbach Susan D, Safiullah Arsalan M, Lalani Seema R, Glass Nancy L, Towbin Jeffrey A, Craigen William J, Belmont John W
Published 2005-02-01