Sampson MG, Coughlin CR 2nd, Kaplan P, Conlin LK, Meyers KE, Zackai EH, Spinner NB, Copelovitch L. Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. Am J Med Genet A. 2010 Oct;152A(10):2618-22. Read abstract.
Collins RT 2nd, Aziz PF, Gleason MM, Kaplan PB, Shah MJ. Abnormalities of cardiac repolarization in Williams syndrome. Am J Cardiol. 2010 Oct 1;106(7):1029-33. Epub 2010 Aug 11. Read abstract.
Collins RT 2nd, Kaplan P, Somes GW, Rome JJ. Long-term outcomes of patients with cardiovascular abnormalities and Williams syndrome. Am J Cardiol. 2010 Mar 15;105(6):874-8. Read abstract
Collins RT 2nd, Kaplan P, Rome JJ. Stenosis of the Thoracic Aorta in Williams Syndrome. Pediatr Cardiol. 2010 Apr 22. [Epub ahead of print]. Read abstract