Works matching IS 01973851 AND DT 2016 AND VI 36 AND IP 13

Results: 20

Are ultrasound renal aspects associated with urinary biochemistry in fetuses with lower urinary tract obstruction?

Published in:

2016

By:

Nassr, Ahmed A.;
Koh, Chester Koh;
Shamshirsaz, Alireza A.;
Espinoza, Jimmy;
Sangi‐Haghpeykar, Haleh;
Sharhan, Dina;
Welty, Stephen;
Angelo, Joseph;
Roth, David;
Belfort, Michael A.;
Braun, Michael;
Ruano, Rodrigo

Publication type:

journal article

Current controversies in prenatal diagnosis 2: for those women screened by NIPT using cell free DNA, maternal serum markers are obsolete.

Published in:

2016

By:

Yaron, Yuval;
Hyett, Jon;
Langlois, Sylvie

Publication type:

journal article

Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction.

Published in:

2016

By:

Kong, Grace Wing Shan;
Cao, Ye;
Huang, Jin;
Cheng, Kwun Yue;
Pursley, Amber Nolen;
Rosenfeld, Jill Anne;
Edwards, Janice G.;
Chan, Yiu Man;
Cheung, Sau Wai;
Leung, Tak Yeung;
Choy, Kwong Wai

Publication type:

journal article

Cover Image, Volume 36, Issue 13.

Published in:

Prenatal Diagnosis, 2016, v. 36, n. 13, p. i, doi. 10.1002/pd.4750

By:

Jarvis, Deborah;
Akram, Rahim;
Mandefield, Laura;
Paddock, Michael;
Armitage, Paul;
Griffiths, Paul D.

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2016, v. 36, n. 13, p. 1159, doi. 10.1002/pd.4751
Publication type:: Article

Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases.

Published in:

2016

By:

Tessier, Aude;
Sarreau, Mélie;
Pelluard, Fanny;
André, Gwenaelle;
Blesson, Sophie;
Bucourt, Martine;
Dechelotte, Pierre;
Faivre, Laurence;
Frébourg, Thierry;
Goldenberg, Alice;
Goua, Valérie;
Jeanne‐Pasquier, Corinne;
Guimiot, Fabien;
Laquerriere, Annie;
Laurent, Nicole;
Lefebvre, Mathilde;
Loget, Philippe;
Maréchaud, Martine;
Mechler, Charlotte;
Perez, Marie‐Josée

Publication type:

journal article

Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.

Published in:

2016

By:

Du, Liu;
Xie, Hong‐Ning;
Huang, Lin‐Huan;
Xie, Ying‐Jun;
Wu, Li‐Hong

Publication type:

journal article

Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.

Published in:

2016

By:

Sukenik‐Halevy, Rivka;
Sukenik, Shay;
Koifman, Arie;
Alpert, Yoav;
Hershkovitz, Reli;
Levi, Alex;
Biron‐Shental, Tal

Publication type:

journal article

The value of the first trimester ultrasound in the era of cell free DNA screening.

Published in:

2016

By:

Rao, Rashmi R.;
Valderramos, Stephanie G.;
Silverman, Neil S.;
Han, Christina S.;
Platt, Lawrence D.

Publication type:

journal article

Prediction of neonatal outcome of TTTS by fetal heart and Doppler ultrasound parameters before and after laser treatment.

Published in:

2016

By:

Delabaere, A.;
Leduc, F.;
Reboul, Q.;
Fuchs, F.;
Wavrant, S.;
Fouron, J. C.;
Audibert, F.

Publication type:

journal article

Current controversies in prenatal diagnosis 1: in utero therapy for spina bifida is ready for endoscopic repair.

Published in:

2016

By:

Belfort, Michael;
Deprest, Jan;
Hecher, Kurt

Publication type:

journal article

Women's choices for invasive or non-invasive testing: influence of gestational age and service delivery.

Published in:

2016

By:

Chen, An;
Tenhunen, Henni;
Torkki, Paulus;
Heinonen, Seppo;
Lillrank, Paul;
Stefanovic, Vedran

Publication type:

journal article

Quantification of total fetal brain volume using 3D MR imaging data acquired in utero.

Published in:

2016

By:

Jarvis, Deborah;
Akram, Rahim;
Mandefield, Laura;
Paddock, Michael;
Armitage, Paul;
Griffiths, Paul D.

Publication type:

journal article

Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.

Published in:

2016

By:

Chen, Ying;
Liu, Yiqian;
Wang, Benjing;
Mao, Jun;
Wang, Ting;
Ye, Kan;
Ye, Yanlin;
Cram, David S.;
Li, Hong

Publication type:

journal article

Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features.

Published in:

2016

By:

Miguet, Marguerite;
Thevenon, Julien;
Laugel, Vincent;
Lefebvre, Mathilde;
Bourchany, Aurélie;
Rivière, Jean‐Baptiste;
Duffourd, Yannis;
Schaefer, Elise;
Antal, Maria Cristina;
Abida, Rosalie;
Weingertner, Anne‐Sophie;
Kremer, Valérie;
Vabres, Pierre;
Morice‐Picard, Fanny;
Gonzales, Marie;
Lipsker, Dan;
Fraitag, Sylvie;
Mandel, Jean‐Louis;
Chelly, Jamel;
Dollfus, Hélène

Publication type:

journal article

Favorable outcomes after in utero transfusion in fetuses with alpha thalassemia major: a case series and review of the literature.

Published in:

2016

By:

Kreger, Emily M.;
Singer, Sylvia T.;
Witt, Russell G.;
Sweeters, Nancy;
Lianoglou, Billie;
Lal, Ashutosh;
Mackenzie, Tippi C.;
Vichinsky, Elliott

Publication type:

journal article

Current controversies in prenatal diagnosis 3: industry drives innovation in research and clinical application of genetic prenatal diagnosis and screening.

Published in:

2016

By:

Evans, Mark I.;
Vermeesch, Joris Robert

Publication type:

journal article

Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.

Published in:

2016

By:

Bayefsky, Michelle J.;
White, Amina;
Wakim, Paul;
Hull, Sara Chandros;
Wasserman, David;
Chen, Stephanie;
Berkman, Benjamin E.

Publication type:

journal article

How many procedures does it take? Success of a CVS training program for Maternal Fetal Medicine fellows.

Published in:

2016

By:

Gimovsky, Alexis C.;
Moreno, Sindy C.;
Nicholas, Sara;
Roman, Amanda;
Weiner, Stuart

Publication type:

journal article

Intra- and inter-observer reproducibility and generalizability of first trimester uterine artery pulsatility index by transabdominal and transvaginal ultrasound.

Published in:

2016

By:

Marchi, Laura;
Zwertbroek, Eva;
Snelder, Judith;
Kloosterman, Maaike;
Bilardo, Caterina Maddalena

Publication type:

journal article