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Inherited and Sporadic Epimutations at the IGF2-H19 Locus in Beckwith-Wiedemann Syndrome and Wilms' Tumor.
- Source :
- Endocrine Development; 2009, Vol. 14, p1-9, 9p
- Publication Year :
- 2009
Details
- Language :
- English
- ISSN :
- 14217082
- Volume :
- 14
- Database :
- Complementary Index
- Journal :
- Endocrine Development
- Publication Type :
- Academic Journal
- Accession number :
- 61437943
- Full Text :
- https://doi.org/10.1159/000207461