Detalhe da pesquisa
1.
Isolation of single circulating trophoblasts from maternal circulation for noninvasive fetal copy number variant profiling.
Prenat Diagn
; 43(1): 14-27, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36443901
2.
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).
Prenat Diagn
; 42(13): 1575-1586, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36403097
3.
Patient experience with non-invasive prenatal testing (NIPT) as a primary screen for aneuploidy in the Netherlands.
BMC Pregnancy Childbirth
; 22(1): 782, 2022 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36266611
4.
Aneuploidy in first trimester chorionic villi and spontaneous abortions: Windows into the origin and fate of aneuploidy through embryonic and fetal development.
Prenat Diagn
; 41(5): 519-524, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32677063
5.
Confirmation rate of cell free DNA screening for sex chromosomal abnormalities according to the method of confirmatory testing.
Prenat Diagn
; 41(10): 1258-1263, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32804406
6.
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
Prenat Diagn
; 41(6): 652-660, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33782989
7.
Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA.
Genet Med
; 22(2): 309-316, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31391534
8.
First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study.
Fetal Diagn Ther
; 47(11): 841-852, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32877902
9.
Noninvasive screening by cell-free DNA for 22q11.2 deletion: Benefits, limitations, and challenges.
Prenat Diagn
; 39(2): 70-80, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30625249
10.
Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus Sampling.
Fetal Diagn Ther
; 46(3): 149-152, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30352439
11.
An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening.
Reprod Biomed Online
; 36(4): 442-449, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29433970
12.
Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
Prenat Diagn
; 37(10): 1017-1027, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28801976
13.
Internalization of nanopolymeric tracers does not alter characteristics of placental cells.
J Cell Mol Med
; 20(6): 1036-48, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26987908
14.
Response to Toutain et al.
Genet Med
; 22(2): 444-445, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31570803
15.
Response to Sistermans et al.
Genet Med
; 22(3): 659-660, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31680122
16.
The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.
Prenat Diagn
; 35(10): 994-8, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26211640
17.
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
Prenat Diagn
; 35(11): 1117-27, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26213308
18.
Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.
Prenat Diagn
; 35(1): 35-43, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25118001
19.
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Prenat Diagn
; 35(8): 801-9, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25962607
20.
De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.
Prenat Diagn
; 34(5): 460-8, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24436202