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Publications by Katherine A. Fawcett

New Genetic Signals for Lung Function Highlight Pathways and Chronic Obstructive Pulmonary Disease Associations Across Multiple Ancestries

Nature 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

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