Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication after introduction of nationwide prenatal screening for trisomy 21, trisomy 13, and trisomy 18

E. H. Steffensen, J. Hyett, O. B. Petersen, I. Vogel, C. Fagerberg, I. Bache, J.F. Hansen, The Danish Cytogenetic Central Registry Study Group

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology