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Publications by Amy E. Roberts
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
Genetics
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
Genetics
A Suggested Role for Mitochondria in Noonan Syndrome
Biochimica et Biophysica Acta - Molecular Basis of Disease
Molecular Medicine
Molecular Biology
Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome
Journal of Pediatrics
Child Health
Pediatrics
Perinatology