Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1
European Journal of Human Genetics (2015) - Comments
pubmed: 25351778  doi: 10.1038/ejhg.2014.230  issn: 1018-4813  issn: 1476-5438 

Laïla El Khattabi, Fabien Guimiot, Eva Pipiras, Joris Andrieux, Clarisse Baumann, Sonia Bouquillon, Anne-Lise Delezoide, Bruno Delobel, Florence Demurger, Hélène Dessuant, Séverine Drunat, Christelle Dubourg, Céline Dupont, Laurence Faivre, Muriel Holder-Espinasse, Sylvie Jaillard, Hubert Journel, Stanislas Lyonnet, Valérie Malan, Alice Masurel