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. Author manuscript; available in PMC: 2020 Jan 28.
Published in final edited form as: Genet Med. 2018 Sep 14;21(3):545–552. doi: 10.1038/s41436-018-0140-3

Fig. 2. Graph plot showing the available OFC (upper panel) and height/length (lower panel) data points at birth and on the last clinical evaluation that we collected for the cohort.

Fig. 2

Red color: Cases with variants in microcephaly primary hereditary (MCPH) genes. Green: Cases with variants in genes with established disease phenotypes in humans with congenital microcephaly (CM). Orange: Cases with variants in genes reported previously as candidate genes. Blue: Cases with variants in genes with no established disease phenotypes in humans. OFC, occipital frontal circumference.