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Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype
✍ Scribed by Sarah T. South; Heidi Whitby; Teresa Maxwell; Emily Aston; Arthur R. Brothman; John C. Carey
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 183 KB
- Volume
- 146A
- Category
- Article
- ISSN
- 1552-4825
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