M. Martí

Xq26.2-q26.3 microduplication in two brothers with intellectual disabilities: clinical and molecular characterization

M. Milá, L. Rodriguez-Revenga, I. Madrigal, 2010, Journal of Human Genetics.

Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

M. Orozco, J. Gelpí, A. Ribes, 2000, Pediatric Research.

What Syndrome Is This?

S. Mallory, B. Hernández, P. Almeida, 2005, Pediatric dermatology.