Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradox - Evers, Christina; Jungwirth, Maria Sophia; Morgenthaler, J.; Hinderhofer, Katrin; Maas, B.; Janssen, Johannes W. G.; Jauch, Anna; Hehr, Ute; Steinbeisser, Herbert; Moog, Ute (Clinical genetics, 2014)
First published: 24 April 2013