Published in

Wiley, Congenital Anomalies, 6(59), p. 195-196, 2019

DOI: 10.1111/cga.12327

Links

Tools

Export citation

Search in Google Scholar

RALA mutation in a patient with autism spectrum disorder and Noonan syndrome‐like phenotype

Journal article published in 2019 by Nobuhiko Okamoto ORCID, Atsushi Takata ORCID, Noriko Miyake, Naomichi Matsumoto
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Upload
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO