Bejjani BA

No ORCID on file · 1 paper in corpus

case-report 2006

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

BMC medical genetics ·doi:10.1186/1471-2350-7-8

BACKGROUND: 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 gr…