Meeting Abstract

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


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

Jahr der Veröffentlichung2023

Seiten597-597

ZeitschriftEuropean Journal of Human Genetics

Bandnummer31

ISSN1018-4813

eISSN1476-5438

Konferenz55th European-Society-of-Human-Genetics (ESHG) Conference

VerlagSpringer Nature [academic journals on nature.com]



Zitierstile

Harvard-ZitierstilLuschka, 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-ZitierstilLuschka, 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.



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