Postyeni E
No ORCID on file
· 1 paper in corpus
· active 2016
Top journals
Frequent coauthors
- Czako M 1
- Duga B 1
- Hadzsiev K 1
- Kosztolanyi G 1
- Komlosi K 1
- Melegh B 1
- Szabo A 1
- Szalai R 1
- Szabo T 1
2016
BackgroundKleefstra syndrome is a rare genetic disorder, with core phenotypic features encompassing developmental delay/intellectual disability, characteristic facial features - brachy(micro)cephaly, unusual shaped eyebrows, flat face with …