The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP.

MLA

Nikkel, Sarah M., et al. “The Phenotype of Floating-Harbor Syndrome: Clinical Characterization of 52 Individuals with Mutations in Exon 34 of SRCAP.” Orphanet Journal of Rare Diseases, vol. 8, no. 1, June 2013, pp. 1–9. EBSCOhost, https://doi.org/10.1186/1750-1172-8-63.

APA

Nikkel, S. M., Dauber, A., De Munnik, S., Connolly, M., Hood, R. L., Caluseriu, O., Hurst, J., Kini, U., Nowaczyk, M. J. M., Afenjar, A., Albrecht, B., Allanson, J. E., Balestri, P., Ben-Omran, T., Brancati, F., Cordeiro, I., Santos da Cunha, B., Delaney, L. A., Destrée, A., & Fitzpatrick, D. (2013). The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. Orphanet Journal of Rare Diseases, 8(1), 1–9. https://doi.org/10.1186/1750-1172-8-63

Chicago

Nikkel, Sarah M., Andrew Dauber, Sonja De Munnik, Meghan Connolly, Rebecca L. Hood, Oana Caluseriu, Jane Hurst, et al. 2013. “The Phenotype of Floating-Harbor Syndrome: Clinical Characterization of 52 Individuals with Mutations in Exon 34 of SRCAP.” Orphanet Journal of Rare Diseases 8 (1): 1–9. doi:10.1186/1750-1172-8-63.