Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
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| Description | article |
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author: Karen E Heath Richard Caswell |
| Publication date | October 18, 2018 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |