Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence?

MLA

Döcker, Dennis, et al. “Germline PTPN11 and Somatic PIK3CA Variant in a Boy with Megalencephaly-Capillary Malformation Syndrome (MCAP)--Pure Coincidence?” European Journal of Human Genetics : EJHG, vol. 23, no. 3, Mar. 2015, pp. 409–12. EBSCOhost, https://doi.org/10.1038/ejhg.2014.118.

APA

Döcker, D., Schubach, M., Menzel, M., Spaich, C., Gabriel, H.-D., Zenker, M., Bartholdi, D., & Biskup, S. (2015). Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence? European Journal of Human Genetics : EJHG, 23(3), 409–412. https://doi.org/10.1038/ejhg.2014.118

Chicago

Döcker, Dennis, Max Schubach, Moritz Menzel, Christiane Spaich, Heinz-Dieter Gabriel, Martin Zenker, Deborah Bartholdi, and Saskia Biskup. 2015. “Germline PTPN11 and Somatic PIK3CA Variant in a Boy with Megalencephaly-Capillary Malformation Syndrome (MCAP)--Pure Coincidence?” European Journal of Human Genetics : EJHG 23 (3): 409–12. doi:10.1038/ejhg.2014.118.