Barbara K Burton

A letter from the SIMD president.

Barbara K Burton, 2008, Molecular genetics and metabolism.

An atypical deletion of the Williams–Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

Uta Francke, Barbara K Burton, U. Francke, 2006, Journal of Medical Genetics.

Phenylalanine hydroxylase deficiency: diagnosis and management guideline

John J. Mitchell, Jerry Vockley, Barbara K Burton, 2013, Genetics in Medicine.

Phenylketonuria Scientific Review Conference: state of the science and future research needs.

Melissa L McPheeters, Mary Lou Lindegren, Anita MacDonald, 2014, Molecular genetics and metabolism.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.