Fig. 1From: A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic featuresClinical features of the patients. Note the facial profile, dolicocephaly and low-set posteriorly rotated ear (a); hypertelorism, low nasal bridge and short philtrum (b); short fifth fingers (c and d)Back to article page