Works matching IS 01973851 AND DT 2021 AND VI 41 AND IP 3

Results: 16

Cover Image.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. ii, doi. 10.1002/pd.5924

By:

Fujibe, Yuya;
Mariya, Tasuku;
Mizuuchi, Masahito

Publication type:

Article

Umbilical cyst associated with patent urachus that spontaneously disappeared: A case report.

Published in:

2021

By:

Fujibe, Yuya;
Mariya, Tasuku;
Mizuuchi, Masahito

Publication type:

Case Study

Cover Image.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. i, doi. 10.1002/pd.5922

By:

Ma, Mary‐Jane L.;
Yakovenko, Sergey;
Zhang, Haiqiang;
Cheng, Suk Hang;
Apryshko, Valentina;
Zhavoronkov, Alex;
Jiang, Peiyong;
Chan, K. C. Allen;
Chiu, Rossa W. K.;
Lo, Y. M. Dennis

Publication type:

Article

Perinatal outcome and prognostic factors of fetal megacystis diagnosed at 11–14 week's gestation.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 308, doi. 10.1002/pd.5868

By:

Kao, Cindy;
Lauzon, Julie;
Brundler, Marie‐Anne;
Tang, Selphee;
Somerset, David

Publication type:

Article

Preclinical stem cell therapy in fetuses with myelomeningocele: A systematic review and meta‐analysis.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 283, doi. 10.1002/pd.5887

By:

Kunpalin, Yada;
Subramaniam, Sindhu;
Perin, Silvia;
Gerli, Mattia F. M.;
Bosteels, Jan;
Ourselin, Sebastien;
Deprest, Jan;
De Coppi, Paolo;
David, Anna L.

Publication type:

Article

Extracardiac Doppler indices predict perinatal mortality in fetuses with Ebstein anomaly and tricuspid valve dysplasia.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 332, doi. 10.1002/pd.5873

By:

Wang, Shuo;
Freud, Lindsay R.;
Detterich, Jon;
Moon‐Grady, Anita J.;
Donofrio, Mary T.;
Jaeggi, Edgar T.;
Szwast, Anita L.;
Morris, Shaine A.;
Kavanaugh‐Mchugh, Ann;
Howley, Lisa W.;
Velde, Mary E.;
Cuneo, Bettina F.;
Phoon, Colin K.;
Tworetzky, Wayne;
Pruetz, Jay D.

Publication type:

Article

Fetal teratomas – A retrospective observational single‐center study.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 301, doi. 10.1002/pd.5872

By:

Simonini, Corinna;
Strizek, Brigitte;
Berg, Christoph;
Gembruch, Ulrich;
Mueller, Andreas;
Heydweiller, Andreas;
Geipel, Annegret

Publication type:

Article

RASopathies: A significant cause of polyhydramnios?

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 362, doi. 10.1002/pd.5862

By:

Mangels, Rachel;
Blumenfeld, Yair J.;
Homeyer, Margaret;
Mrazek‐Pugh, Barbora;
Hintz, Susan R.;
Hudgins, Louanne

Publication type:

Article

Fetal mitochondrial DNA in maternal plasma in surrogate pregnancies: Detection and topology.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 368, doi. 10.1002/pd.5860

By:

Ma, Mary‐Jane L.;
Yakovenko, Sergey;
Zhang, Haiqiang;
Cheng, Suk Hang;
Apryshko, Valentina;
Zhavoronkov, Alex;
Jiang, Peiyong;
Chan, K. C. Allen;
Chiu, Rossa W. K.;
Lo, Y. M. Dennis

Publication type:

Article

Socioeconomic barriers to prenatal diagnosis of critical congenital heart disease.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 341, doi. 10.1002/pd.5864

By:

Campbell, Matthew J.;
Lorch, Scott;
Rychik, Jack;
Quartermain, Michael D.;
Passarella, Molly;
Groeneveld, Peter W.

Publication type:

Article

Exploring the predicted yield of prenatal testing by evaluating a postnatal population with structural abnormalities using a novel mathematical model.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 354, doi. 10.1002/pd.5858

By:

Nunley, Peyton B.;
Hashmi, Syed S.;
Johnson, Anthony;
Ashfaq, Myla;
Farach, Laura S.;
Singletary, Claire N.;
Stevens, Blair K.

Publication type:

Article

Ultrasound detected prenatal hyperechoic lung lesions and concordance with postnatal findings: A common aspect for multiple diagnoses.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 323, doi. 10.1002/pd.5854

By:

Wong, Michela Cing Yu;
Faure Bardon, Valentine;
Farmakis, Konstantinos;
Berteloot, Laureline;
Lapillonne, Alexandre;
Delacourt, Christophe;
Sarnacki, Sabine;
Ville, Yves;
Khen‐Dunlop, Naziha

Publication type:

Article

Personalized prenatal genomic testing: Couples' experience with choice regarding uncertain and adult‐onset findings from chromosomal‐microarray‐analysis.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 376, doi. 10.1002/pd.5856

By:

Millo, Talya;
Douiev, Liza;
Popper, Dov;
Shkedi‐Rafid, Shiri

Publication type:

Article

Prenatally detected isolated ventricular septum defects and the association with chromosomal aberrations—A nationwide register‐based study from Denmark.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 347, doi. 10.1002/pd.5853

By:

Vedel, Cathrine;
Rode, Line;
Jørgensen, Finn Stener;
Petersen, Olav Bjørn;
Sundberg, Karin;
Tabor, Ann;
Ekelund, Charlotte Kvist

Publication type:

Article

Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 3, p. 316, doi. 10.1002/pd.5834

By:

Zhang, Wenwen;
Lei, Tingying;
Fu, Fang;
Deng, Qiong;
Li, Ru;
Wang, Dan;
Yang, Xin;
Li, Dongzhi;
Liao, Can

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2021, v. 41, n. 3, p. 281, doi. 10.1002/pd.5740
Publication type:: Article