APA (7th ed.) Citation

Marchetto, A., Leidescher, S., van Hoi, T., Hirschberger, N., Vogel, F., Köhler, S., . . . Keil, C. (2024). Prenatal Diagnosis of Fryns Syndrome through Identification of Two Novel Splice Variants in the PIGN Gene—A Case Series. Life (2075-1729), 14(5), 628. https://doi.org/10.3390/life14050628

Chicago Style (17th ed.) Citation

Marchetto, Aruna, et al. "Prenatal Diagnosis of Fryns Syndrome Through Identification of Two Novel Splice Variants in the PIGN Gene—A Case Series." Life (2075-1729) 14, no. 5 (2024): 628. https://doi.org/10.3390/life14050628.

MLA (9th ed.) Citation

Marchetto, Aruna, et al. "Prenatal Diagnosis of Fryns Syndrome Through Identification of Two Novel Splice Variants in the PIGN Gene—A Case Series." Life (2075-1729), vol. 14, no. 5, 2024, p. 628, https://doi.org/10.3390/life14050628.