학술논문
All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience
Document Type
Article
Author
Faas, B.H.W.; Westra, D.; de Munnik, S.A.; van Rij, M.; Marcelis, C.; Joosten, S.; Willemsen, M.H.; de Leeuw, N.; Rinne, T.; Pfundt, R.; Smeekens, S.P.; Derks, I.; Hofste, T.; Timmermans, R.; van den End, J.; Feenstra, I.; Krapels, I.; Vernimmen, V.; Heijligers, M.; Stegmann, S.P.A.; Macville, M.; van Lent-Albrechts, J.; Stevens, S.J.C.; Sikkel, E.; Coumans, A.; Wijnberger, L.
Source
In: Prenatal Diagnosis . (Prenatal Diagnosis, April 2023, 43(4):527-543)
Subject
Language
English
ISSN
10970223
01973851
01973851