Meyer, R., & Opladen, T. (2021). One test for all: Whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver-Russell syndrome. Orphanet journal of rare diseases, 16, . https://doi.org/10.1186/s13023-021-01683-x
Chicago-Zitierstil (17. Ausg.)Meyer, Robert, und Thomas Opladen. "One Test for All: Whole Exome Sequencing Significantly Improves the Diagnostic Yield in Growth Retarded Patients Referred for Molecular Testing for Silver-Russell Syndrome." Orphanet Journal of Rare Diseases 16 (2021). https://doi.org/10.1186/s13023-021-01683-x.
MLA-Zitierstil (9. Ausg.)Meyer, Robert, und Thomas Opladen. "One Test for All: Whole Exome Sequencing Significantly Improves the Diagnostic Yield in Growth Retarded Patients Referred for Molecular Testing for Silver-Russell Syndrome." Orphanet Journal of Rare Diseases, vol. 16, 2021, https://doi.org/10.1186/s13023-021-01683-x.