Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial (Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2
Year: 2001
Type: article
Study design: Observational Study
Source: European Journal of Pediatrics
Institutions: University of Zurich, Luzerner Kantonsspital, Kantonsspital Aarau
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W1992590929
