✦ LIBER ✦
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
✍ Scribed by 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
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 275 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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