Detalhe da pesquisa
1.
Performance of a cell-free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low-risk cell-free DNA screening.
Prenat Diagn
; 43(2): 213-225, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36617980
2.
Ethical issues associated with prenatal screening using non-invasive prenatal testing for sex chromosome aneuploidy.
Prenat Diagn
; 43(2): 226-234, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35929376
3.
Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies.
Clin Chem
; 67(9): 1210-1219, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34077512
4.
Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study.
Am J Obstet Gynecol
; 225(5): 527.e1-527.e12, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33957116
5.
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Hum Reprod
; 35(3): 694-704, 2020 03 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32207823
6.
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016.
Prenat Diagn
; 39(13): 1254-1261, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31691307
7.
'Is it better not to know certain things?': views of women who have undergone non-invasive prenatal testing on its possible future applications.
J Med Ethics
; 45(4): 231-238, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30679192
8.
'Small cost to pay for peace of mind': Women's experiences with non-invasive prenatal testing.
Aust N Z J Obstet Gynaecol
; 59(5): 649-655, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30724335
9.
Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies.
Prenat Diagn
; 43(7): 814-828, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37076973
10.
A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin.
J Obstet Gynaecol Res
; 44(5): 955-959, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29436108
11.
Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.
BMC Med
; 14(1): 126, 2016 08 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27558279
12.
International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies.
Prenat Diagn
; 41(10): 1222-1232, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33016373
13.
The clinical benefit of genome-wide cfDNA testing cannot be extrapolated from CVS data.
Genet Med
; 22(3): 657-658, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31690836
14.
Rapid evolution of mouse Y centromere repeat DNA belies recent sequence stability.
Genome Res
; 19(12): 2202-13, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19737860
15.
Cancer Diagnoses Following Abnormal Noninvasive Prenatal Testing: A Case Series, Literature Review, and Proposed Management Model.
JCO Precis Oncol
; 5: 1001-1012, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34994626
16.
Maternal mosaicism for a large segmental duplication of 18q as a secondary finding following non-invasive prenatal testing and implications for test accuracy.
Prenat Diagn
; 35(10): 986-9, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26151667
17.
Harmonizing Cell-Free DNA Collection and Processing Practices through Evidence-Based Guidance.
Clin Cancer Res
; 26(13): 3104-3109, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32122922
18.
First trimester detection of trisomy 16 using combined biochemical and ultrasound screening.
Prenat Diagn
; 34(3): 291-5, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24353252
19.
Isolation and Characterization of Mesenchymal Stem/Stromal Cells Derived from Human Third Trimester Placental Chorionic Villi and Decidua Basalis.
Methods Mol Biol
; 1710: 247-266, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29197008
20.
Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome.
Eur J Hum Genet
; 26(10): 1490-1496, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29899373