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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
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2010)
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