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Interstitial deletion of 16q has emerged into a recognizable pattern of congenital malformation. We report on a 9‐year‐old boy with short stature, psychomotor retardation, high forehead, broad flat nasal bridge, hypertelorism, cup‐shaped ears, short neck, and a normal karyotype. Using high‐density oligonucleotide array chip (Affymetrix 6.0) to perform parental and proband samples concurrently on three...
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