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Strauss, Kevin

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Item Type	Name
Concept	Craniofacial Abnormalities
Academic Article	Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions.
Academic Article	CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease.

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