Article

Comparing 2D and 3D representations for face-based genetic syndrome diagnosis

2023-02-07

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: cadffb73-ace8-5912-b834-b213ec14ff87
DOI: 10.1038/s41431-023-01308-w

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Comparing 2D and 3D representations for face-based genetic syndrome diagnosisDOI 10.1038/s41431-023-01308-wRead

Facial analysis technology aids diagnoses of genetic disorders: applications narrow down potential genetic syndromes by matching facial phenotypes to distinct set of possible genetic conditions.Semantic proximity Read

Computational facial analysis for rare Mendelian disorders.Semantic proximity Read

Population-specific facial traits and diagnosis accuracy of genetic and rare diseases in an admixed Colombian populationSemantic proximity Read

Discriminating power of localized three-dimensional facial morphology.Semantic proximity Read

Diagnostically relevant facial gestalt information from ordinary photos.Semantic proximity Read

Population-specific facial traits and diagnosis accuracy of genetic and rare diseases in an admixed Colombian populationSemantic proximity Read

Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes.Semantic proximity Read

Facial malformation atlas aims to aid diagnosis of genetic disorders in patients of non-European descent: National Human Genome Research Institute launches online database of facial phenotypes targeting diverse populations.Semantic proximity Read

Population-specific facial traits and diagnosis accuracy of genetic and rare diseases in an admixed Colombian population.Semantic proximity Read

3D phenotyping in a Colombian population reveals unique population and ontogenic facial patterns in genetic and rare disordersSemantic proximity Read

Next generation phenotyping in Emanuel and Pallister-Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos.Semantic proximity Read

Development and evaluation of a machine learning-based point-of-care screening tool for genetic syndromes in children: a multinational retrospective study.Semantic proximity Read