✦ LIBER ✦
Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome
✍ Scribed by Swati Naik; Elliott Riordan-Eva; N. Simon Thomas; Rebecca Poole; Mark Ashton; John A. Crolla; I. Karen Temple
- Book ID
- 116433311
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 616 KB
- Volume
- 54
- Category
- Article
- ISSN
- 1769-7212
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