Meeting Abstract

Detection of Turner Syndrome in newborn screening: validation of a fragment-analysis based approach


Authors listLuschka, Ruth; Bedei, Ivonne; Becker-Follmann, Johannes; Weber, Axel; Agirman, Zeynep; Khairi-Taraki, Tarrin; Schaefer, Ramon Enriquez; Axt-Fliedner, Roland

Publication year2023

Pages597-597

JournalEuropean Journal of Human Genetics

Volume number31

ISSN1018-4813

eISSN1476-5438

Conference55th European-Society-of-Human-Genetics (ESHG) Conference

PublisherSpringer Nature [academic journals on nature.com]



Citation Styles

Harvard Citation styleLuschka, R., Bedei, I., Becker-Follmann, J., Weber, A., Agirman, Z., Khairi-Taraki, T., et al. (2023) Detection of Turner Syndrome in newborn screening: validation of a fragment-analysis based approach, European Journal of Human Genetics, 31, p. 597

APA Citation styleLuschka, R., Bedei, I., Becker-Follmann, J., Weber, A., Agirman, Z., Khairi-Taraki, T., Schaefer, R., & Axt-Fliedner, R. (2023). Detection of Turner Syndrome in newborn screening: validation of a fragment-analysis based approach. European Journal of Human Genetics. 31, 597.


Last updated on 2025-21-05 at 18:09