Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
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
5.
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
6.
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
7.
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications.
Prenat Diagn
; 36(12): 1146-1155, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27770451
8.
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
9.
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
10.
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
11.
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
12.
Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results.
Genet Med
; 16(8): 620-4, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24525917
13.
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
14.
Fetal mesenchymal stromal cells from cryopreserved human chorionic villi: cytogenetic and molecular analysis of genome stability in long-term cultures.
Cytotherapy
; 15(11): 1340-51, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24094486
15.
Response: how PGS/PGT-A laboratories succeeded in losing all credibility.
Reprod Biomed Online
; 37(2): 246, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30075842
16.
Response: scoring of mosaic embryos after preimplantation genetic testing - the rollercoaster ride between fear, hope and embryo wastage.
Reprod Biomed Online
; 37(1): 122, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754985
17.
Application of a new molecular technique for the genetic evaluation of products of conception.
Prenat Diagn
; 33(1): 32-41, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23168908
18.
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.
Prenat Diagn
; 33(5): 502-8, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23606546
19.
Prenatal BACs-on-Beads™: the prospective experience of five prenatal diagnosis laboratories.
Prenat Diagn
; 32(4): 329-35, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22467163
20.
Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes.
Am J Med Genet A
; 152A(6): 1434-42, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20503318