A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation
Crossref DOI link: https://doi.org/10.1007/s00381-017-3646-0
Published Online: 2017-10-24
Published Print: 2018-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Tan, Ai Peng http://orcid.org/0000-0001-7660-6322
Mankad, Kshitij
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