✦ LIBER ✦
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith–Wiedemann syndrome
✍ Scribed by Agostina De Crescenzo; Filomena Coppola; Pietro Falco; Italo Bernardo; Gaetano Ausanio; Flavia Cerrato; Luigi Falco; Andrea Riccio
- Book ID
- 116433395
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 346 KB
- Volume
- 54
- Category
- Article
- ISSN
- 1769-7212
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