V. L. R. Tavares

Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect

B. Papsin, J. T. Dunnen, H. Buermans, 2015, European Journal of Human Genetics.

Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21‐22.1 locus

M. Passos-Bueno, P. Prontera, C. Sobacchi, 2011, American journal of medical genetics. Part A.