✦ LIBER ✦
Microdeletion 11q13.1.q13.2 in a patient presenting with developmental delay, facial dysmorphism, and esophageal atresia: Possible role of the GSTP1 gene in esophagus malformation
✍ Scribed by Ferreira de Almeida, Tatiana; Bertola, Débora Romeo
- Book ID
- 126853803
- Publisher
- John Wiley and Sons
- Year
- 2013
- Tongue
- English
- Weight
- 61 KB
- Volume
- 97
- Category
- Article
- ISSN
- 1542-0752
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