Kjaer, K., Hansen, L., Schwabe, G., Marques-de-Faria, A., Eiberg, H., Mundlos, S., . . . Rosenberg, T. (2005). Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome). BMJ Group.
Citação norma ChicagoKjaer, K., L. Hansen, G. Schwabe, A. Marques-de-Faria, H. Eiberg, S. Mundlos, N. Tommerup, and T. Rosenberg. Distinct CDH3 Mutations Cause Ectodermal Dysplasia, Ectrodactyly, Macular Dystrophy (EEM Syndrome). BMJ Group, 2005.
MLA citiranjeKjaer, K., et al. Distinct CDH3 Mutations Cause Ectodermal Dysplasia, Ectrodactyly, Macular Dystrophy (EEM Syndrome). BMJ Group, 2005.
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