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38 results on '"FEDERICO MAGGI"'

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1. Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies

2. Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications

3. Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis

4. The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure

5. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

6. Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies

7. De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches

8. QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses

9. Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications

10. Application of a new molecular technique for the genetic evaluation of products of conception

11. Prenatal BACs-on-Beads™ : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis

12. Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH

13. The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure

14. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

15. Prenatal search for UPD 14 and UPD 15 in 83 cases of familial andde novo heterologous Robertsonian translocations

16. 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?

17. De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches

18. FIRST-TRIMESTER CHROMOSOME DIAGNOSIS BY LAVAGE OF THE UTERINE CAVITY

19. Application of a new molecular technique for the genetic evaluation of products of conception

20. Response to 'QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44 727 first-trimester prenatal diagnoses'

21. False-positive and false-negative findings on chorionic villus sampling

23. Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.

24. Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications.

25. Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.

26. The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.

27. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.

30. De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.

32. QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses.

33. Application of a new molecular technique for the genetic evaluation of products of conception.

38. Response to 'QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44 727 first-trimester prenatal diagnoses'.

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