Figure 1From: A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation Family pedigree and dysmophic features observed. A) Family pedigree identifying the proband as II-3. Dysmorphic features found in the proband included B) webbing of the neck and C) fifth finger clinodactyly. D) X-ray of hands and wrists showed evidence of osteoporosis and clinodactyly.Back to article page