Cite
HARVARD Citation
Gordon, C. et al. (2018). MED13L loss‐of‐function variants in two patients with syndromic Pierre Robin sequence. American journal of medical genetics. 176 (1), pp. 181-186. [Online].
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Gordon, C. et al. (2018). MED13L loss‐of‐function variants in two patients with syndromic Pierre Robin sequence. American journal of medical genetics. 176 (1), pp. 181-186. [Online].