Works matching IS 01973851 AND DT 2022 AND VI 42 AND IP 7

Results: 18

Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 934, doi. 10.1002/pd.6159

By:

Buchanan, James;
Hill, Melissa;
Vass, Caroline M.;
Hammond, Jennifer;
Riedijk, Sam;
Klapwijk, Jasmijn E.;
Harding, Eleanor;
Lou, Stina;
Vogel, Ida;
Hui, Lisa;
Ingvoldstad‐Malmgren, Charlotta;
Soller, Maria Johansson;
Ormond, Kelly E.;
Choolani, Mahesh;
Zheng, Qian;
Chitty, Lyn S.;
Lewis, Celine

Publication type:

Article

Cover Image.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 1, doi. 10.1002/pd.6198

By:

Liu, Pengfei;
Vossaert, Liesbeth

Publication type:

Article

Fetal phenotypes of Mendelian disorders: A descriptive study from India.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 911, doi. 10.1002/pd.6172

By:

Saini, Neelam;
Venkatapuram, Vijaya Sree;
Vineeth, Venugopal Satidevi;
Kulkarni, Aditya;
Tandon, Ashwani;
Koppolu, Gayatri;
Patil, Siddaramappa Jagdish;
Dalal, Ashwin;
Aggarwal, Shagun

Publication type:

Article

Prenatal diagnosis for fetuses with isolated and non‐isolated congenital heart defects using chromosomal microarray and exome sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 873, doi. 10.1002/pd.6168

By:

Xing, Ya;
Zhang, Yun;
Chen, Jianping;
Wu, Fengyu;
Yuan, Meizhen;
Zou, Gang;
Yang, Yingjun;
Zhou, Fenhe;
Zhou, Jia;
Sun, Luming

Publication type:

Article

A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 901, doi. 10.1002/pd.6170

By:

Dufke, Andreas;
Hoopmann, Markus;
Waldmüller, Stephan;
Prodan, Natalia Carmen;
Beck‐Wödl, Stefanie;
Grasshoff, Ute;
Heinrich, Tilman;
Riess, Angelika;
Kehrer, Martin;
Falb, Ruth J.;
Liebmann, Alexandra;
Roggia, Cristiana;
Stampfer, Miriam;
Schadeck, Malou;
Müller, Amelie J.;
Grimmel, Mona;
Stöbe, Petra;
Gauck, Darja;
Buchert‐Lo, Rebecca;
Baumann, Sarah

Publication type:

Article

Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 927, doi. 10.1002/pd.6171

By:

Rinaldi, Berardo;
Cesaretti, Claudia;
Boito, Simona;
Villa, Roberta;
Guerneri, Silvana;
Borzani, Irene;
Rizzuti, Tommaso;
Marchetti, Daniela;
Conte, Giorgio;
Cinnante, Claudia;
Triulzi, Fabio;
Persico, Nicola;
Iascone, Maria;
Natacci, Federica

Publication type:

Article

The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 807, doi. 10.1002/pd.6190

By:

Giordano, Jessica L.;
Wapner, Ronald J.

Publication type:

Article

Lessons learnt from prenatal exome sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 831, doi. 10.1002/pd.6165

By:

Chandler, Natalie J.;
Scotchman, Elizabeth;
Mellis, Rhiannon;
Ramachandran, Vijaya;
Roberts, Rowenna;
Chitty, Lyn S.

Publication type:

Article

Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 894, doi. 10.1002/pd.6154

By:

Liu, Ling;
Li, Juan;
Li, Ying;
Li, Haiyu;
Yang, Bo;
Fan, Hui;
Wang, Jing;
Gu, Yanting;
Yu, Hui;
Bai, Maohuan;
Yu, Tantan;
Cui, Shihong;
Cheng, Guomei;
Ren, Chenchen

Publication type:

Article

Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 862, doi. 10.1002/pd.6151

By:

Cao, Y.;
Chau, M. H. K.;
Zheng, Y.;
Zhao, Y.;
Kwan, A. H. W.;
Hui, S. Y. A.;
Lam, Y. H.;
Tan, T. Y. T.;
Tse, W. T.;
Wong, L.;
Leung, T. Y.;
Dong, Z.;
Choy, K. W.

Publication type:

Article

Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 947, doi. 10.1002/pd.6153

By:

Kernie, Catherine G.;
Wynn, Julia;
Rosenbaum, Allison;
de Voest, Jessica;
Galloway, Stephanie;
Giordano, Jessica;
Stover, Samantha;
Westerfield, Lauren;
Gilmore, Kelly;
Wapner, Ronald J.;
Van den Veyver, Ignatia B.;
Vora, Neeta L.;
Clifton, Rebecca G.;
Caughey, Aaron B.;
Chung, Wendy K.

Publication type:

Article

Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 811, doi. 10.1002/pd.6144

By:

Zemet, Roni;
Van den Veyver, Ignatia B.;
Stankiewicz, Paweł

Publication type:

Article

Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 890, doi. 10.1002/pd.6142

By:

Reytan, Sivan;
Zunz Henig, Noa;
Yinon, Yoav;
Avnet, Hagai;
Kurolap, Alina;
Yaron, Yuval;
Baris Feldman, Hagit

Publication type:

Article

Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 822, doi. 10.1002/pd.6108

By:

Wang, Yiming;
Greenfeld, Elena;
Watkins, Nicholas;
Belesiotis, Peter;
Zaidi, Syed H.;
Marshall, Christian;
Thiruvahindrapuram, Bhooma;
Shannon, Patrick;
Roifman, Maian;
Chong, Karen;
Chitayat, David;
Stavropoulos, Dimitri James;
Noor, Abdul

Publication type:

Article

Trio exome sequencing is highly relevant in prenatal diagnostics.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 845, doi. 10.1002/pd.6081

By:

Gabriel, Heinz;
Korinth, Dirk;
Ritthaler, Martin;
Schulte, Björn;
Battke, Florian;
von Kaisenberg, Constantin;
Wüstemann, Max;
Schulze, Bernt;
Friedrich‐Freksa, Almuth;
Pfeiffer, Lutz;
Entezami, Michael;
Schröer, Andreas;
Bürger, Joachim;
Schwaibold, Eva Maria Christina;
Lebek, Holger;
Biskup, Saskia

Publication type:

Article

Diagnostic yield of whole exome data in fetuses aborted for conotruncal malformations.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 852, doi. 10.1002/pd.6147

By:

Shi, Jia‐wei;
Cao, Haiyan;
Hong, Liu;
Ma, Jing;
Cui, Li;
Zhang, Yi;
Song, Xiaoyan;
Liu, Juanjuan;
Yang, Yali;
Lv, Qing;
Zhang, Li;
Wang, Jing;
Xie, Mingxing

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2022, v. 42, n. 7, p. 805, doi. 10.1002/pd.5964
Publication type:: Article

The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 881, doi. 10.1002/pd.5977

By:

Wagner, Tova;
Fahham, Duha;
Frumkin, Ayala;
Shaag, Avraham;
Yagel, Simcha;
Yanai, Nili;
Porat, Shay;
Mor‐Shaked, Hagar;
Meiner, Vardiella;
Daum, Hagit

Publication type:

Article