Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array.

MLA

Iordănescu, Irina Ioana, et al. “Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array.” Journal of Personalized Medicine, vol. 14, no. 3, Mar. 2024, p. 290. EBSCOhost, https://doi.org/10.3390/jpm14030290.

APA

Iordănescu, I. I., Catana, A., Cuzmici, Z. B., Chelu, I., Dragomir, C., Militaru, M., Severin, E., & Militaru, M. S. (2024). Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array. Journal of Personalized Medicine, 14(3), 290. https://doi.org/10.3390/jpm14030290

Chicago

Iordănescu, Irina Ioana, Andreea Catana, Zina Barabas Cuzmici, Iuliana Chelu, Cristina Dragomir, Maria Militaru, Emilia Severin, and Mariela Sanda Militaru. 2024. “Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array.” Journal of Personalized Medicine 14 (3): 290. doi:10.3390/jpm14030290.