Aarskog-Scott syndrome: a novel mutation in the FGD1 gene associated with severe craniofacial dysplasia
Crossref DOI link: https://doi.org/10.1007/s00431-014-2317-3
Published Online: 2014-04-27
Published Print: 2014-10
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Völter, Christiane
Martínez, Ramón
Hagen, Rudolf
Kress, Wolfram
Text and Data Mining valid from 2014-04-27