(Q56332951)
Statements
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 (English)
M R Passos-Bueno
1 reference
F S Jehee
K M Rocha
D P Cavalcanti
J F Mazzeu
G Froyen
D Lugtenberg
A M Vianna-Morgante