Bisschoff, I. J., & Evers, C. (2013). Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: A study of the extensive clinical variability. Human mutation, 34(1), . https://doi.org/https://doi.org/10.1002/humu.22224
Chicago-Zitierstil (17. Ausg.)Bisschoff, Izak Johannes, und Christina Evers. "Novel Mutations Including Deletions of the Entire OFD1 Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability." Human Mutation 34, no. 1 (2013). https://doi.org/https://doi.org/10.1002/humu.22224.
MLA-Zitierstil (9. Ausg.)Bisschoff, Izak Johannes, und Christina Evers. "Novel Mutations Including Deletions of the Entire OFD1 Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability." Human Mutation, vol. 34, no. 1, 2013, https://doi.org/https://doi.org/10.1002/humu.22224.