Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders. [electronic resource]
Producer: 20200206Description: 1719-1725 p. digitalISSN:- 1530-0366
- Abnormalities, Multiple -- diagnosis
- Adolescent
- Adult
- Algorithms
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 17 -- genetics
- Craniofacial Abnormalities -- diagnosis
- Facial Recognition
- Female
- Genomics
- Humans
- Image Processing, Computer-Assisted
- Infant
- Intellectual Disability -- diagnosis
- Intracellular Signaling Peptides and Proteins -- genetics
- Male
- Middle Aged
- Muscular Atrophy -- diagnosis
- Musculoskeletal Abnormalities -- diagnosis
- Mutation, Missense -- genetics
- Neurodevelopmental Disorders -- diagnosis
- Phenotype
- Protein Phosphatase 2C -- genetics
- Vesicular Transport Proteins -- genetics
- Young Adult
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.