Concurrent maternal malignancy and fetal trisomy detected using genome-wide noninvasive prenatal screening
Prenat Diagn
.
2021 Sep;41(10):1273-1276.
doi: 10.1002/pd.6020.
Epub 2021 Aug 14.
Authors
Fergus Scott
1
2
,
Maria-Elisabeth Smet
1
3
,
Tristan Hardy
4
,
Samantha Sundercombe
5
,
Michael Friedlander
2
6
,
Louise Carey
5
7
,
Edwin Kirk
5
7
,
Biao Li
8
,
Andrew McLennan
1
9
Affiliations
1
Sydney Ultrasound for Women, Sydney, Australia.
2
University of New South Wales, Sydney, Australia.
3
Fetal Medicine Unit, Westmead Hospital, Sydney, Australia.
4
Repromed, SA Pathology, Adelaide, Australia.
5
NSW Health Pathology Randwick Genomics, Randwick, Australia.
6
Department of Medical Oncology, Prince of Wales Clinical School, The Prince of Wales Hospital, Sydney, Australia.
7
School of Women's and Children's Health, UNSW, Sydney Children's Hospital, Randwick, Australia.
8
Department of Bioinformatics, Illumina Inc., San Diego, CA, USA.
9
Discipline of Obstetrics, Gynaecology and Neonatology, The University of Sydney, Sydney, Australia.
PMID:
34318961
DOI:
10.1002/pd.6020
No abstract available
MeSH terms
Adult
Female
Humans
Neoplasms / diagnosis*
Neoplasms / epidemiology
Pregnancy
Prenatal Diagnosis / methods*
Prenatal Diagnosis / trends
Trisomy / diagnosis*
Trisomy / genetics
Trisomy / physiopathology