المؤلفون: Pizzo, Lucilla, Jensen, Matthew, Polyak, Andrew, Rosenfeld, Jill A., Mannik, Katrin, Krishnan, Arjun, McCready, Elizabeth, Pichon, Olivier, Le Caignec, Cedric, Van Dijck, Anke, Pope, Kate, Voorhoeve, Els, Yoon, Jieun, Stankiewicz, Pawel, Cheung, Sau Wai, Pazuchanics, Damian, Huber, Emily, Kumar, Vijay, Kember, Rachel L., Mari, Francesca, Curro, Aurora, Castiglia, Lucia, Galesi, Ornella, Avola, Emanuela, Mattina, Teresa, Fichera, Marco, Mandara, Luana, Vincent, Marie, Nizon, Mathilde, Mercier, Sandra, Beneteau, Claire, Blesson, Sophie, Martin-Coignard, Dominique, Mosca-Boidron, Anne-Laure, CABERG, Jean-Hubert, Bucan, Maja, Zeesman, Susan, Nowaczyk, Malgorzata J. M., Lefebvre, Mathilde, Faivre, Laurence, Callier, Patrick, Skinner, Cindy, Keren, Boris, Perrine, Charles, Prontera, Paolo, Marle, Nathalie, Renieri, Alessandra, Reymond, Alexandre, Kooy, R. Frank, Isidor, Bertrand, Schwartz, Charles, Romano, Corrado, Sistermans, Erik, Amor, David J., Andrieux, Joris, Girirajan, Santhosh

المصدر: Genetics in Medicine (2019)

مصطلحات موضوعية: 16p11.2 deletion, CNV, autism, modifier, phenotypic variability, Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques

العلاقة: urn:issn:1098-3600; urn:issn:1530-0366; https://orbi.uliege.be/handle/2268/230063Test; info:hdl:2268/230063; scopus-id:2-s2.0-85053071043; info:pmid:30190612

الإتاحة: https://doi.org/10.1038/s41436-018-0266-3Test
https://orbi.uliege.be/handle/2268/230063Test

المؤلفون: Ho, Boey S., McCready, Elizabeth, Nowaczyk, Malgorzata J. M.

المصدر: Clinical Dysmorphology; Jul2016, Vol. 25 Issue 3, p128-132, 5p