TY  - GEN
AU  - van der Donk,Roos
AU  - Jansen,Sandra
AU  - Schuurs-Hoeijmakers,Janneke H M
AU  - Koolen,David A
AU  - Goltstein,Lia C M J
AU  - Hoischen,Alexander
AU  - Brunner,Han G
AU  - Kemmeren,Patrick
AU  - Nellåker,Christoffer
AU  - Vissers,Lisenka E L M
AU  - de Vries,Bert B A
AU  - Hehir-Kwa,Jayne Y
TI  - Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders
SN  - 1530-0366
PY  - 2020///0206
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Adolescent
KW  - Adult
KW  - Algorithms
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 17
KW  - genetics
KW  - Craniofacial Abnormalities
KW  - Facial Recognition
KW  - Female
KW  - Genomics
KW  - Humans
KW  - Image Processing, Computer-Assisted
KW  - Infant
KW  - Intellectual Disability
KW  - Intracellular Signaling Peptides and Proteins
KW  - Male
KW  - Middle Aged
KW  - Muscular Atrophy
KW  - Musculoskeletal Abnormalities
KW  - Mutation, Missense
KW  - Neurodevelopmental Disorders
KW  - Phenotype
KW  - Protein Phosphatase 2C
KW  - Vesicular Transport Proteins
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/s41436-018-0404-y
ER  -