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Phenotypic similarity for rare disease: Ciliopathy diagnoses and subtyping.

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Title: Phenotypic similarity for rare disease: Ciliopathy diagnoses and subtyping.
Authors: Chen, Xiaoyi1, xiaoyi.chen@inserm.fr, Garcelon, Nicolas2, Neuraz, Antoine1,3, Billot, Katy4,5, Lelarge, Marc6, Bonald, Thomas7, Garcia, Hugo4,5, Martin, Yoann4,5, Benoit, Vincent2, Vincent, Marc2, Faour, Hassan2, Douillet, Maxime2, Lyonnet, Stanislas5,8,9, Saunier, Sophie4,5, Burgun, Anita1,3,5
Source: Journal of Biomedical Informatics; Dec2019, Vol. 100, pN.PAG-N.PAG, 1p
Database: Applied Science & Technology Source
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Header DbId: aci
DbLabel: Applied Science & Technology Source
An: 140096197
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=140096197
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        Value: 10.1016/j.jbi.2019.103308
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      – Code: eng
        Text: English
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      – TitleFull: Phenotypic similarity for rare disease: Ciliopathy diagnoses and subtyping.
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              Text: Dec2019
              Type: published
              Y: 2019
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