(Q84966043)
Statements
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 (English)
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
1 September 2010