Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
Population-based trends in the prenatal diagnosis of sex chromosome aneuploidy before and after non-invasive prenatal testing.
Prenat Diagn
; 38(13): 1062-1068, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30255507
5.
Prenatal and preimplantation genetic diagnosis for single gene disorders: A population-based study from 1977 to 2016.
Prenat Diagn
; 38(12): 904-910, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30184264
6.
Prenatal diagnosis and socioeconomic status in the non-invasive prenatal testing era: A population-based study.
Aust N Z J Obstet Gynaecol
; 58(4): 404-410, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29380343
7.
Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy.
Genet Med
; 19(12): 1338-1345, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28518169
8.
Family Communication about Diagnostic Genetic Testing for Younger-Onset Dementia.
J Pers Med
; 13(4)2023 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37109007