High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation
F S Jehee, A C V Krepischi-Santos, K M Rocha, D P Cavalcanti, C A Kim, D R Bertola, L G Alonso, C S DAngelo, J F Mazzeu, G Froyen, D Lugtenberg, A M Vianna-Morgante, C Rosenberg, and M R Passos-Bueno