[Next-generation phenotyping in rare diseases with facial dysmorphism]
Inn Med (Heidelb)
.
2023 Nov;64(11):1041-1043.
doi: 10.1007/s00108-023-01616-9.
Epub 2023 Oct 19.
[Article in German]
Author
Peter Krawitz
1
Affiliation
1
Institut für Genomische Statistik und Bioinformatik (IGSB), Universitätsklinikum Bonn (AöR), Venusberg-Campus 1, 53127, Bonn, Deutschland. pkrawitz@uni-bonn.de.
PMID:
37855883
DOI:
10.1007/s00108-023-01616-9
No abstract available
Publication types
Review
MeSH terms
Humans
Musculoskeletal Abnormalities*
Rare Diseases* / diagnosis