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Pathogenic variants in USP7 cause a neurodevelopmental diso..:
Fountain, Michael D
;
Oleson, David S
;
Rech, Megan E
...
qt0h47s4s0. , 2019
Link:
https://escholarship.org/uc/item/0h47s4s0
RT Journal T1
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt0h47s4s0&Exemplar=1&LAN=DE A1 Fountain, Michael D A1 Oleson, David S A1 Rech, Megan E A1 Segebrecht, Lara A1 Hunter, Jill V A1 McCarthy, John M A1 Lupo, Philip J A1 Holtgrewe, Manuel A1 Moran, Rocio A1 Rosenfeld, Jill A A1 Isidor, Bertrand A1 Le Caignec, Cédric A1 Saenz, Margarita S A1 Pedersen, Robert C A1 Morgan, Thomas M A1 Pfotenhauer, Jean P A1 Xia, Fan A1 Bi, Weimin A1 Kang, Sung-Hae L A1 Patel, Ankita A1 Krantz, Ian D A1 Raible, Sarah E A1 Smith, Wendy A1 Cristian, Ingrid A1 Torti, Erin A1 Juusola, Jane A1 Millan, Francisca A1 Wentzensen, Ingrid M A1 Person, Richard E A1 Küry, Sébastien A1 Bézieau, Stéphane A1 Uguen, Kévin A1 Férec, Claude A1 Munnich, Arnold A1 van Haelst, Mieke A1 Lichtenbelt, Klaske D A1 van Gassen, Koen A1 Hagelstrom, Tanner A1 Chawla, Aditi A1 Perry, Denise L A1 Taft, Ryan J A1 Jones, Marilyn A1 Masser-Frye, Diane A1 Dyment, David A1 Venkateswaran, Sunita A1 Li, Chumei A1 Escobar, Luis F A1 Horn, Denise A1 Spillmann, Rebecca C A1 Peña, Loren A1 Wierzba, Jolanta A1 Strom, Tim M A1 Parenti, Ilaria A1 Kaiser, Frank J A1 Ehmke, Nadja A1 Schaaf, Christian P PB eScholarship, University of California YR 2019 K1 Biological Sciences K1 Genetics K1 Brain Disorders K1 Neurosciences K1 Behavioral and Social Science K1 Clinical Research K1 Pediatric K1 Congenital Structural Anomalies K1 Intellectual and Developmental Disabilities (IDD) K1 Mental Health K1 Autism K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adolescent K1 Autism Spectrum Disorder K1 Child K1 Preschool K1 Chromosome Deletion K1 DNA-Binding Proteins K1 Genome K1 Human K1 Haploinsufficiency K1 Humans K1 Infant K1 Newborn K1 Intellectual Disability K1 Language Development Disorders K1 Neurodevelopmental Disorders K1 Nuclear Proteins K1 Phenotype K1 Problem Behavior K1 Proteins K1 Exome Sequencing K1 USP7 K1 neurodevelopment K1 speech delay K1 white matter paucity K1 corpus callosum thinning K1 Clinical Sciences K1 Genetics & Heredity JF qt0h47s4s0 LK http://dx.doi.org/https://escholarship.org/uc/item/0h47s4s0 DO https://escholarship.org/uc/item/0h47s4s0 SF ELIB - SuUB Bremen
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