Fountain, Michael D. https://orcid.org/0000-0002-2148-7490
Oleson, David S.
Rech, Megan E.
Segebrecht, Lara
Hunter, Jill V.
McCarthy, John M.
Lupo, Philip J.
Holtgrewe, Manuel
Moran, Rocio
Rosenfeld, Jill A.
Isidor, Bertrand
Le Caignec, Cédric
Saenz, Margarita S.
Pedersen, Robert C.
Morgan, Thomas M.
Pfotenhauer, Jean P.
Xia, Fan
Bi, Weimin
Kang, Sung-Hae L.
Patel, Ankita
Krantz, Ian D.
Raible, Sarah E.
Smith, Wendy
Cristian, Ingrid
Torti, Erin
Juusola, Jane
Millan, Francisca
Wentzensen, Ingrid M.
Person, Richard E.
Küry, Sébastien
Bézieau, Stéphane
Uguen, Kévin
Férec, Claude
Munnich, Arnold
van Haelst, Mieke
Lichtenbelt, Klaske D.
van Gassen, Koen
Hagelstrom, Tanner
Chawla, Aditi
Perry, Denise L.
Taft, Ryan J.
Jones, Marilyn
Masser-Frye, Diane
Dyment, David
Venkateswaran, Sunita
Li, Chumei
Escobar, Luis F.
Horn, Denise
Spillmann, Rebecca C.
Peña, Loren
Wierzba, Jolanta
Strom, Tim M.
Parenti, Ilaria
Kaiser, Frank J.
Ehmke, Nadja
Schaaf, Christian P.
This article is maintained by: Elsevier
Article Title: Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0433-1
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics