dysmorphic mild 16p11 displays duplication prominent triangular bulbous
16p11 deletion individuals developmental delay
microdeletion representative individuals
facial preterm deletion infant diagnostic distal
22q11 patients deletions typical atypical deletion publication vcfs nasal mouth
chromosome disorder interstitial powerpoint 1q21
deletion syndrome gene open proximal repeats copy low homologous recombination non figure bp1 bp4 allelic deletions policy copyright access jmg
canal mri findings deletion dilated 16p11 publication dilatation syrinx t1