TY  - GEN
AU  - Ockeloen,Charlotte W
AU  - Willemsen,Marjolein H
AU  - de Munnik,Sonja
AU  - van Bon,Bregje W M
AU  - de Leeuw,Nicole
AU  - Verrips,Aad
AU  - Kant,Sarina G
AU  - Jones,Elizabeth A
AU  - Brunner,Han G
AU  - van Loon,Rosa L E
AU  - Smeets,Eric E J
AU  - van Haelst,Mieke M
AU  - van Haaften,Gijs
AU  - Nordgren,Ann
AU  - Malmgren,Helena
AU  - Grigelioniene,Giedre
AU  - Vermeer,Sascha
AU  - Louro,Pedro
AU  - Ramos,Lina
AU  - Maal,Thomas J J
AU  - van Heumen,Celeste C
AU  - Yntema,Helger G
AU  - Carels,Carine E L
AU  - Kleefstra,Tjitske
TI  - Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
SN  - 1476-5438
PY  - 2016///0524
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Adolescent
KW  - Adult
KW  - Autism Spectrum Disorder
KW  - complications
KW  - Bone Diseases, Developmental
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 16
KW  - DNA Mutational Analysis
KW  - Exome
KW  - Facies
KW  - Female
KW  - Gene Deletion
KW  - Gene Expression
KW  - Genotype
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Middle Aged
KW  - Phenotype
KW  - Repressor Proteins
KW  - genetics
KW  - Tooth Abnormalities
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ejhg.2014.253
ER  -