van der Donk, Roos <br/><br/>
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics  08 2019 
 - 1719-1725 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1530-0366 
<br/><br/><label>Standard No.: </label>10.1038/s41436-018-0404-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Adult<br/>Algorithms<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--genetics<br/>Craniofacial Abnormalities--diagnosis<br/>Facial Recognition<br/>Female<br/>Genomics<br/>Humans<br/>Image Processing, Computer-Assisted<br/>Infant<br/>Intellectual Disability--diagnosis<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Male<br/>Middle Aged<br/>Muscular Atrophy--diagnosis<br/>Musculoskeletal Abnormalities--diagnosis<br/>Mutation, Missense--genetics<br/>Neurodevelopmental Disorders--diagnosis<br/>Phenotype<br/>Protein Phosphatase 2C--genetics<br/>Vesicular Transport Proteins--genetics<br/>Young Adult