Cite
p53+/mdm2- Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma in Young Children: An Early Expression of Li-Fraumeni Syndrome.
MLA
Debelenko, Larisa V., et al. “P53+/Mdm2- Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma in Young Children: An Early Expression of Li-Fraumeni Syndrome.” Pediatric & Developmental Pathology, vol. 13, no. 3, May 2010, pp. 218–24. EBSCOhost, https://doi.org/10.2350/09-08-0694-OA.1.
APA
Debelenko, L. V., Perez-Atayde, A. R., Dubois, S. G., Grier, H. E., Sung-Yun Pai, Shamberger, R. C., & Kozakewich, H. P. W. (2010). p53+/mdm2- Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma in Young Children: An Early Expression of Li-Fraumeni Syndrome. Pediatric & Developmental Pathology, 13(3), 218–224. https://doi.org/10.2350/09-08-0694-OA.1
Chicago
Debelenko, Larisa V., Antonio R. Perez-Atayde, Steven G. Dubois, Holcombe E. Grier, Sung-Yun Pai, Robert C. Shamberger, and Harry P. W. Kozakewich. 2010. “P53+/Mdm2- Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma in Young Children: An Early Expression of Li-Fraumeni Syndrome.” Pediatric & Developmental Pathology 13 (3): 218–24. doi:10.2350/09-08-0694-OA.1.