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Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder.
Clin Genet. 2015 Sep;88(3):224-33. doi: 10.1111/cge.12482. Epub 2014 Oct 14.
Clin Genet. 2015.
PMID: 25131214
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
Noor A, Lionel AC, Cohen-Woods S, Moghimi N, Rucker J, Fennell A, Thiruvahindrapuram B, Kaufman L, Degagne B, Wei J, Parikh SV, Muglia P, Forte J, Scherer SW, Kennedy JL, Xu W, McGuffin P, Farmer A, Strauss J, Vincent JB.
Noor A, et al. Among authors: degagne b.
Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):303-13. doi: 10.1002/ajmg.b.32232. Epub 2014 Apr 3.
Am J Med Genet B Neuropsychiatr Genet. 2014.
PMID: 24700553
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Spatial Frequency Thresholds for Detecting Latent Facial Signals of Threat.
Watier N, DeGagne B.
Watier N, et al. Among authors: degagne b.
Perception. 2019 Mar;48(3):214-227. doi: 10.1177/0301006619828254. Epub 2019 Feb 6.
Perception. 2019.
PMID: 30727834
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