Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency
Crossref DOI link: https://doi.org/10.1186/s13633-017-0047-9
Published Online: 2017-08-04
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Giri, Dinesh
Rigden, Daniel
Didi, Mohammed
Peak, Matthew
McNamara, Paul
Senniappan, Senthil