Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome

Ching Fen Chang, Ling Hui Li, Chung Hsing Wang, Fuu Jen Tsai, Tsai Chuan Chen, Jer Yuarn Wu, Yuan Tsong Chen, Anne Chun Hui Tsai

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