TY  - GEN
AU  - Low,Karen
AU  - Ashraf,Tazeen
AU  - Canham,Natalie
AU  - Clayton-Smith,Jill
AU  - Deshpande,Charu
AU  - Donaldson,Alan
AU  - Fisher,Richard
AU  - Flinter,Frances
AU  - Foulds,Nicola
AU  - Fryer,Alan
AU  - Gibson,Kate
AU  - Hayes,Ian
AU  - Hills,Alison
AU  - Holder,Susan
AU  - Irving,Melita
AU  - Joss,Shelagh
AU  - Kivuva,Emma
AU  - Lachlan,Kathryn
AU  - Magee,Alex
AU  - McConnell,Vivienne
AU  - McEntagart,Meriel
AU  - Metcalfe,Kay
AU  - Montgomery,Tara
AU  - Newbury-Ecob,Ruth
AU  - Stewart,Fiona
AU  - Turnpenny,Peter
AU  - Vogt,Julie
AU  - Fitzpatrick,David
AU  - Williams,Maggie
AU  - Smithson,Sarah
TI  - Clinical and genetic aspects of KBG syndrome
SN  - 1552-4833
PY  - 2017///1019
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Bone Diseases, Developmental
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 16
KW  - Comparative Genomic Hybridization
KW  - Facies
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Intellectual Disability
KW  - Male
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/10.1002/ajmg.a.37842
ER  -