Duga B

No ORCID on file · 1 paper in corpus · active 2016
2016
Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype.
Molecular cytogenetics ·doi:10.1186/s13039-016-0231-2

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 …