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3. Application of a new molecular technique for the genetic evaluation of products of conception. (20th November 2012)

5. De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches. (11th February 2014)

6. Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high‐risk indications. (18th November 2016)

7. Implications of fetoplacental mosaicism on cell‐free DNA testing for sex chromosome aneuploidies. (6th September 2017)

8. Increased risk after noninvasive prenatal screening on cell‐free DNA circulating in maternal blood: does a new indication for invasive prenatal diagnosis require new criteria for confirmatory cytogenetic analysis?. (March 2015)

9. Increased risk after noninvasive prenatal screening on cell‐free DNA circulating in maternal blood: does a new indication for invasive prenatal diagnosis require new criteria for confirmatory cytogenetic analysis?. (March 2015)

10. Internalization of nanopolymeric tracers does not alter characteristics of placental cells. Issue 6 (14th March 2016)