✦ LIBER ✦
Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth
✍ Scribed by Dan Hanson; Philip G. Murray; James O'Sullivan; Jill Urquhart; Sarah Daly; Sanjeev S. Bhaskar; Leslie G. Biesecker; Mars Skae; Claire Smith; Trevor Cole; Jeremy Kirk; Kate Chandler; Helen Kingston; Dian Donnai; Peter E. Clayton; Graeme C.M. Black
- Book ID
- 113423062
- Publisher
- American Society of Human Genetics
- Year
- 2011
- Tongue
- English
- Weight
- 784 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0002-9297
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