Works matching IS 01973851 AND DT 2018 AND VI 38 AND IP 10

Results: 17

Ethical and counseling challenges in prenatal exome sequencing.

Published in:

2018

By:

Harris, Sarah;
Gilmore, Kelly;
Hardisty, Emily;
Lyerly, Anne Drapkin;
Vora, Neeta L

Publication type:

journal article

Impact of prenatal diagnosis of complex congenital heart disease on neonatal and infant morbidity and mortality.

Published in:

2018

By:

Chakraborty, Abhishek;
Gorla, Sudheer R;
Swaminathan, Sethuraman

Publication type:

journal article

Cover Image, Volume 38, Issue 10.

Published in:: Prenatal Diagnosis, 2018, v. 38, n. 10, p. i, doi. 10.1002/pd.5341
Publication type:: Article

Corrigendum for Arya, Bhat, Vernon, et al. (2015) https://doi.org/10.1002/pd.4753.

Published in:

2018

By:

Arya, Bhawna;
Bhat, Aarti;
Vernon, Margaret;
Conwell, Jeffrey;
Lewin, Mark

Publication type:

journal article

Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.

Published in:

2018

By:

Li, Duan;
Lin, Yunting;
Huang, Yonglan;
Zhang, Wen;
Jiang, Minyan;
Li, Xiuzhen;
Zhao, Xiaoyuan;
Sheng, Huiying;
Yin, Xi;
Su, Xueying;
Shao, Yongxian;
Liu, Zongcai;
Li, Dongzhi;
Li, Fatao;
Liao, Can;
Liu, Li

Publication type:

journal article

Perinatal outcomes following cell-free DNA screening in >32 000 women: Clinical follow-up data from a single tertiary center.

Published in:

2018

By:

Liang, Dong;
Lin, Ying;
Qiao, Fengchang;
Li, Hang;
Wang, Yan;
Zhang, Jingjing;
Liu, An;
Ji, Xiuqing;
Ma, Dingyuan;
Jiang, Tao;
Hu, Ping;
Xu, Zhengfeng

Publication type:

journal article

Rare autosomal trisomies: Important and not so rare.

Published in:

2018

By:

Scott, Fergus;
Bonifacio, Michael;
Sandow, Rhiannon;
Ellis, Katie;
Smet, Maria‐Elisabeth;
McLennan, Andrew;
Smet, Maria-Elisabeth

Publication type:

journal article

Prenatal chromosomal microarray uptake with invasive prenatal diagnosis: How many patients take the leap?

Published in:

2018

By:

Singletary, Claire N.;
Krstic, Nevena Cvjetkovic;
Czerwinski, Jennifer L.;
Choates, Meagan Giles;
Wagner, Chelsea

Publication type:

journal article

Impacts of variants of uncertain significance on parental perceptions of children after prenatal chromosome microarray testing.

Published in:

2018

By:

Desai, Preeya;
Haber, Hannah;
Bulafka, Jessica;
Russell, Amita;
Clifton, Rebecca;
Zachary, Julia;
Lee, Seonjoo;
Feng, Tianshu;
Wapner, Ronald;
Monk, Catherine;
Chung, Wendy K.

Publication type:

journal article

Echocardiographic predictors of neonatal illness severity in fetuses with critical left heart obstruction with intact or restrictive atrial septum.

Published in:

2018

By:

Gellis, Laura;
Drogosz, Monika;
Lu, Minmin;
Sleeper, Lynn A.;
Cheng, Henry;
Allan, Catherine;
Marshall, Audrey C.;
Tworetzky, Wayne;
Friedman, Kevin G.

Publication type:

journal article

Fetal cerebral hemorrhage due to X-linked GATA1 gene mutation.

Published in:

2018

By:

Bouchghoul, Hanane;
Quelin, Chloé;
Loget, Philippe;
Encha‐Razavi, Féréchté;
Senat, Marie‐Victoire;
Maheut, Lorraine;
Galimand, Julie;
Collardeau‐Frachon, Sophie;
Da Costa, Lydie;
Martinovic, Jelena;
Encha-Razavi, Féréchté;
Senat, Marie-Victoire;
Collardeau-Frachon, Sophie

Publication type:

journal article

Response to comment on "Utility of novel fetal echocardiographic morphometric measures of the aortic arch in the diagnosis of neonatal coarctation of the aorta".

Published in:

2018

By:

Arya, Bhawna

Publication type:

Letter

Trends in invasive prenatal diagnostic testing at a single institution.

Published in:

2018

By:

Awomolo, Adeola;
Palomares, Kristy;
Garcia, Guadalupe Herrera;
Rosen, Todd;
Duzyj, Christina;
Ashkinadze, Elena

Publication type:

journal article

Comment on "Utility of novel fetal echocardiographic morphometric measures of the aortic arch in the diagnosis of neonatal coarctation of the aorta".

Published in:

2018

By:

DeVore, Greggory R.

Publication type:

Letter

Missed diagnoses of abnormal copy number variant cases: A national epidemic or an endemic at a single institution?

Published in:

2018

By:

Ghidini, Alessandro;
Chitty, Lyn S.

Publication type:

Editorial

The epidemic of abnormal copy number variant cases missed because of reliance upon noninvasive prenatal screening.

Published in:

2018

By:

Evans, Mark I.;
Andriole, Stephanie;
Curtis, Jenifer;
Evans, Shara M.;
Kessler, Alan A.;
Rubenstein, Andrew F.

Publication type:

journal article

Issue Information.

Published in:: Prenatal Diagnosis, 2018, v. 38, n. 10, p. 725, doi. 10.1002/pd.5130
Publication type:: Article