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Publications by Andrew E. Fry

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

American Journal of Human Genetics

English

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

American Journal of Human Genetics

English

Exome Sequencing in Crisponi/CISS-like Individuals Reveals Unpredicted Alternative Diagnoses

Clinical Genetics

English