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You searched for: Author/Creator Demko, Z.

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1. Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome. (5th January 2016)

3. OC11.01: *Clinical experience with carrier screening in a general population: support for a comprehensive pan‐ethnic approach. (15th October 2020)

4. OP09.05: Prediction of pre‐eclampsia using machine learning. (14th September 2022)