Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
Crossref DOI link: https://doi.org/10.1007/s13353-017-0408-3
Published Online: 2017-09-21
Published Print: 2017-11
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Tumiene, Birute http://orcid.org/0000-0001-6010-2584
Čiuladaitė, Ž.
Preikšaitienė, E.
Mameniškienė, R.
Utkus, A.
Kučinskas, V.
License valid from 2017-09-21