Article Versions Notes

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

Marchetto, Aruna, Susanne Leidescher, Theresia van Hoi, Niklas Hirschberger, Florian Vogel, Siegmund Köhler, Ivonne Alexandra Bedei, Roland Axt-Fliedner, Moneef Shoukier, and Corinna Keil. 2024. "Prenatal Diagnosis of Fryns Syndrome through Identification of Two Novel Splice Variants in the PIGN Gene—A Case Series" Life 14, no. 5: 628. https://doi.org/10.3390/life14050628

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