Works matching IS 01973851 AND DT 2021 AND VI 41 AND IP 10

Results: 23

Low fetal fraction in cell‐free DNA testing is associated with adverse pregnancy outcome: Analysis of a subcohort of the TRIDENT‐2 study.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1296, doi. 10.1002/pd.6034

By:

Becking, Ellis C.;
Wirjosoekarto, Soetinah A. M.;
Scheffer, Peter G.;
Huiskes, Julia V. M.;
Remmelink, Marinka J.;
Sistermans, Erik A.;
Bax, Caroline J.;
Weiss, Janneke M.;
Henneman, Lidewij;
Bekker, Mireille N.

Publication type:

Article

Non-invasive prenatal testing 10 years on.

Published in:

2021

By:

Chitty, Lyn S

Publication type:

Editorial

Non‐invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1264, doi. 10.1002/pd.6031

By:

Lannoo, Lore;
Lenaerts, Liesbeth;
Van Den Bogaert, Kris;
Che, Huiwen;
Brison, Nathalie;
Devriendt, Koen;
Amant, Frédéric;
Vermeesch, Joris Robert;
Van Calsteren, Kristel

Publication type:

Article

Diagnostic testing after positive results on cell free DNA screening: CVS or Amnio?

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1249, doi. 10.1002/pd.6021

By:

Mardy, Anne H;
Norton, Mary E.

Publication type:

Article

Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1351, doi. 10.1002/pd.6003

By:

de Groot‐van der Mooren, Maurike;
de Graaf, Gert;
Weijerman, Michel E;
Hoffer, Mariette J. V;
Knijnenburg, Jeroen;
van der Kevie‐Kersemaekers, Anne‐Marie M. F;
Kooper, Angelique J. A;
Voorhoeve, Els;
Sikkema‐Raddatz, Birgit;
van Zutven, Laura J. C. M;
Srebniak, Malgorzata Ilona;
Huijsdens‐van Amsterdam, Karin;
Engelen, John J. M;
Smeets, Dominique;
van Kaam, Anton H;
Cornel, Martina C

Publication type:

Article

Overview and recent developments in cell‐based noninvasive prenatal testing.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1202, doi. 10.1002/pd.5957

By:

Vossaert, Liesbeth;
Chakchouk, Imen;
Zemet, Roni;
Van den Veyver, Ignatia B.

Publication type:

Article

The potential of expanded noninvasive prenatal screening for detection of microdeletion and microduplication syndromes.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1332, doi. 10.1002/pd.6002

By:

Shi, Panlai;
Wang, Yuan;
Liang, Hongbin;
Hou, Yaqin;
Chen, Duo;
Zhao, Ganye;
Dai, Peng;
Xia, Yanjie;
Feng, Yin;
Cram, David S.;
Kong, Xiangdong

Publication type:

Article

Association between low fetal fraction in cell‐free DNA testing and adverse pregnancy outcome: A systematic review.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1287, doi. 10.1002/pd.6028

By:

Scheffer, Peter G.;
Wirjosoekarto, Soetinah A. M.;
Becking, Ellis C.;
Weiss, Marjan M.;
Bax, Caroline J.;
Oepkes, Dick;
Sistermans, Erik A.;
Henneman, Lidewij;
Bekker, Mireille N.

Publication type:

Article

Low fetal fraction in obese women at first trimester cell‐free DNA based prenatal screening is not accompanied by differences in total cell‐free DNA.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1277, doi. 10.1002/pd.6023

By:

Shree, Raj;
Kolarova, Teodora R.;
MacKinnon, Hayley J.;
Hedge, Jaclynne M.;
Vinopal, Elena;
Ma, Kimberly K.;
Lockwood, Christina M.;
Chandrasekaran, Suchitra

Publication type:

Article

Increased nuchal translucency after low‐risk noninvasive prenatal testing: What should we tell prospective parents?

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1305, doi. 10.1002/pd.6024

By:

Kelley, Joanne;
McGillivray, George;
Meagher, Simon;
Hui, Lisa

Publication type:

Article

Knowledge and attitudes regarding non‐invasive prenatal testing among women in Saudi Arabia.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1343, doi. 10.1002/pd.5991

By:

Bawazeer, Shahad;
AlSayed, Moeenaldeen;
Kurdi, Wesam;
Balobaid, Ameera

Publication type:

Article

Concurrent maternal malignancy and fetal trisomy detected using genome‐wide noninvasive prenatal screening.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1273, doi. 10.1002/pd.6020

By:

Scott, Fergus;
Smet, Maria‐Elisabeth;
Hardy, Tristan;
Sundercombe, Samantha;
Friedlander, Michael;
Carey, Louise;
Kirk, Edwin;
Li, Biao;
McLennan, Andrew

Publication type:

Article

Non‐invasive prenatal testing in the management of twin pregnancies.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1233, doi. 10.1002/pd.5989

By:

Benn, Peter;
Rebarber, Andrei

Publication type:

Article

Noninvasive prenatal testing: Advancing through a virtuous circle of science, technology and clinical applications.

Published in:

2021

By:

Lo, Y M Dennis

Publication type:

journal article

Cell‐free DNA analysis of maternal blood in prenatal screening for chromosomal microdeletions and microduplications: a systematic review.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1324, doi. 10.1002/pd.5928

By:

Familiari, Alessandra;
Boito, Simona;
Rembouskos, Georgios;
Ischia, Benedetta;
Accurti, Veronica;
Fabietti, Isabella;
Volpe, Paolo;
Persico, Nicola

Publication type:

Article

Current controversies in prenatal diagnosis: Expanded NIPT that includes conditions other than trisomies 13, 18, and 21 should be offered.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1316, doi. 10.1002/pd.5943

By:

Christiaens, Lieve;
Chitty, Lyn S.;
Langlois, Sylvie

Publication type:

Article

Increased RISK for 47,XXY on cell‐free DNA screen: Not always Klinefelter syndrome.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1255, doi. 10.1002/pd.5890

By:

Ronzoni, Luisa;
Bedeschi, Maria Francesca;
Silibello, Gaia;
Accurti, Veronica;
Di Segni, Marina;
Nicotra, Valeria;
Vizziello, Paola;
Lalatta, Faustina

Publication type:

Article

Should vanishing twin pregnancies be systematically excluded from cell‐free fetal DNA testing?

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1241, doi. 10.1002/pd.5817

By:

Balaguer, Nuria;
Mateu‐Brull, Emilia;
Serra, Vicente;
Simón, Carlos;
Milán, Miguel

Publication type:

Article

Economic impact of using maternal plasma cell‐free DNA testing to guide further workup in recurrent pregnancy loss.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1215, doi. 10.1002/pd.5972

By:

Peng, Siyang;
Bhatt, Sucheta;
Borrell, Antoni;
Yaron, Yuval

Publication type:

Article

Cell‐free fetal DNA coming in all sizes and shapes.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1193, doi. 10.1002/pd.5952

By:

Chiu, Rossa W. K.;
Lo, Y.M. Dennis

Publication type:

Article

Confirmation rate of cell free DNA screening for sex chromosomal abnormalities according to the method of confirmatory testing.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1258, doi. 10.1002/pd.5814

By:

Lüthgens, Kai;
Grati, Francesca Romana;
Sinzel, Monika;
Häbig, Karina;
Kagan, Karl Oliver

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1185, doi. 10.1002/pd.5747
Publication type:: Article

International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1222, doi. 10.1002/pd.5832

By:

Palomaki, Glenn E.;
Chiu, Rossa W.K.;
Pertile, Mark D.;
Sistermans, Erik A.;
Yaron, Yuval;
Vermeesch, Joris Robert;
Vora, Neeta L.;
Best, Robert G.;
Wilkins‐Haug, Louise

Publication type:

Article