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File:CDK13-related disorder Hamilton 2.png

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An individual with CDK13-related disorder

Summary

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Description
English: An individual with CDK13-related disorder, showing the characteristic facial appearance
Date
Source Hamilton, Mark J; Caswell, Richard C; Canham, Natalie; Cole, Trevor; Firth, Helen V; Foulds, Nicola; Heimdal, Ketil; Hobson, Emma; Houge, Gunnar; Joss, Shelagh; Kumar, Dhavendra (January 2018). "Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability". Journal of Medical Genetics. 55 (1): 28–38. doi:10.1136/jmedgenet-2017-104620. ISSN 0022-2593. PMC 5749303. PMID 29021403.
Annotated label "P5" was removed by User:SUM1.
Author Hamilton et al.


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current17:19, 2 December 2019Thumbnail for version as of 17:19, 2 December 2019798 × 1,013 (482 KB)SUM1 (talk | contribs)User created page with UploadWizard

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