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s12881-017-0501-9
s12881-017-0501-9
https://scigraph.springernature.com/pub.10.1186/s12881-017-0501-9
Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review.
P2888
Q47102023-D8F6BE8A-68F6-46AA-B5A7-6B80E609BD80
P2888
s12881-017-0501-9
https://scigraph.springernature.com/pub.10.1186/s12881-017-0501-9