Lenglet, M., Robriquet, F., Schwarz, K., Camps, C., Couturier, A., Hoogewijs, D., . . . Gardie, B. (2018). Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease. American Society of Hematology.
Chicagoスタイル(17版)引用形式Lenglet, M., et al. Identification of a New VHL Exon and Complex Splicing Alterations in Familial Erythrocytosis or Von Hippel-Lindau Disease. American Society of Hematology, 2018.
MLA(9版)引用形式Lenglet, M., et al. Identification of a New VHL Exon and Complex Splicing Alterations in Familial Erythrocytosis or Von Hippel-Lindau Disease. American Society of Hematology, 2018.
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