Rejane A C Monteiro

Holoprosencephaly, orofacial cleft, and frontonaso‐orbital encephaloceles: Genetic evaluation of a possible new syndrome

L. Hoefsloot, Siulan Vendramini-Pittoli, R. M. Candido-Souza, 2019, American journal of medical genetics. Part A.

Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use of MLPA as the First Genetic Test

F. Jehee, J. Mazzeu, G. Vianna, 2017, Molecular Syndromology.

Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes

F. Jehee, G. Vianna, E. Mateo, 2016, Molecular Syndromology.

Contents Vol. 7, 2016

M. Mussini, M. Poot, Siulan Vendramini-Pittoli, 2016, Molecular Syndromology.