Works matching IS 01973851 AND DT 2024 AND VI 44 AND IP 11

Results: 17

Characterization of the Prenatal Ultrasound Phenotype Associated With 7q11.23 Microduplication Syndrome and Williams–Beuren Syndrome.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1398, doi. 10.1002/pd.6669

By:

Wang, Fengyang;
Peng, Huijuan;
Lou, Guiyu;
Ren, Yanxin;
Liao, Shixiu

Publication type:

Article

Reversal of Fetal Compromise Following In Utero Treatment of Vein of Galen Malformation Using Glue.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1367, doi. 10.1002/pd.6662

By:

Gowda, Mamatha;
Krishnaraj, Ariharan;
Ambalakkuthan, Murugesan;
Chinta, Navya;
Selvan, Tamil

Publication type:

Article

Lethal Skeletal Dysplasia in Fetus With Novel COL1A1 Variant.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1412, doi. 10.1002/pd.6652

By:

Wang, Michelle J.;
Schioppo, Davia;
Donovan, Bridget M.;
Febres‐Cordero, Daniela A.;
Connolly, Susan;
Robinson, Julian;
Duffy, Cassandra R.

Publication type:

Article

Imaging‐Based Prediction Parameters of Perinatal Morbidity and Mortality for Fetal Occipital Cephaloceles.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1327, doi. 10.1002/pd.6660

By:

Gaulden, Amber L.;
Nagaraj, Usha D.;
Emmert, A. Scott;
Vuong, Shawn M.;
Kline‐Fath, Beth M.;
Bierbrauer, Karin S.;
Patel, Smruti K.

Publication type:

Article

Agenesis of Corpus Callosum, Malformations of Cortical Development, Duodenal Atresia and Fetal Growth Restriction: Prenatal Markers for Zhu‐Tokita‐Takenouchi‐Kim Syndrome.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1416, doi. 10.1002/pd.6658

By:

Carmant, Laurence Sophie;
Miller, Elka;
Chong, Karen;
Chitayat, David;
Shinar, Shiri

Publication type:

Article

Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1296, doi. 10.1002/pd.6657

By:

Burnett, Brian;
Parobek, Christian;
Shanahan, Matthew;
Mitts, Matthew;
Albrecht, Kelly;
Munoz, Jessian L.;
Buskmiller, Cara;
Nassar, Ahmed A.;
Sanz Cortes, Magdalena;
Belfort, Michael A.;
Donepudi, Roopali V.

Publication type:

Article

The Conundrum of Mechanics Versus Genetics in Congenital Hydrocephalus and Its Implications for Fetal Therapy Approaches: A Scoping Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1354, doi. 10.1002/pd.6654

By:

Herzeg, Akos;
Borges, Beltran;
Diafos, Loukas N.;
Gupta, Nalin;
MacKenzie, Tippi C.;
Sanders, Stephan J.

Publication type:

Article

SNPscan Combined With CNVplex as a High‐Performance Diagnostic Method for Thalassemia.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1310, doi. 10.1002/pd.6661

By:

Wei, Xiaofeng;
Wang, Xingmin;
Xiong, Fu;
Zhang, Xinhua;
Liu, Dun;
Zhou, Wanjun;
He, Fei;
Shang, Xuan

Publication type:

Article

Maternal cell contamination in postnatal umbilical cord blood samples implies a low risk for genetic misdiagnoses.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1304, doi. 10.1002/pd.6595

By:

Smeekens, Sanne P.;
Leferink, Maike.;
Yntema, Helger G.;
Kamsteeg, Erik‐Jan

Publication type:

Article

Experimental Induction of Complex Gastroschisis in the Fetal Lamb: Systematic Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1372, doi. 10.1002/pd.6647

By:

Arai, Tomohiro;
Tianthong, Wasinee;
Russo, Francesca Maria;
Basurto, David;
Joyeux, Luc;
De Coppi, Paolo;
Deprest, Jan

Publication type:

Article

The Reliability of Ultrasound Markers in Identifying Fetuses With a Life‐Limiting Skeletal Dysplasia.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1318, doi. 10.1002/pd.6638

By:

Crane, Haley M.;
Schindewolf, Erica;
Burrill, Natalie;
Debari, Suzanne;
Khalek, Nahla;
Paidas Teefey, Christina;
Soni, Shelly;
Coleman, Beverly;
Moldenhauer, Julie S.;
Gebb, Juliana

Publication type:

Article

Prenatal Phenotype of Alkuraya‐Kučinskas Syndrome: A Novel Case and Systematic Literature Review.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1381, doi. 10.1002/pd.6637

By:

Rice, Stephanie M.;
Varotsis, Dante F.;
Wodoslawsky, Sascha;
Critchlow, Elizabeth;
Liu, Ruby;
McLaren, Rodney A.;
Makhamreh, Mona M.;
Firman, Brandy;
Berger, Seth I.;
Al‐Kouatly, Huda B.

Publication type:

Article

Customizing carrier screening in the Chinese population: Insights from a 334‐gene panel.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1335, doi. 10.1002/pd.6635

By:

Liu, Sha;
Huang, Shuang;
Zhang, Victor Wei;
Cao, Liyuan;
Liu, Haipeng;
Wei, Xiang;
Luo, Yuan;
Li, Yue;
Zhou, Lin;
Li, Fuping;
Zhu, Qian;
Liu, Hongqian

Publication type:

Article

Exome sequencing in fetuses with congenital diaphragmatic hernia in a nationwide cohort.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1288, doi. 10.1002/pd.6622

By:

Weller, Katinka;
Westra, Dineke;
Peters, Nina C. J.;
Wilke, Martina;
Van Opstal, Diane;
Feenstra, Ilse;
van Drongelen, Joris;
Eggink, Alex J.;
Diderich, Karin E. M.;
DeKoninck, Philip L. J.

Publication type:

Article

Asian Screening Array and Next‐Generation Sequencing Based Panels Applied to Preimplantation Genetic Testing for Monogenic Disorders Preclinical Workup in 294 Families: A Retrospective Analysis.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1344, doi. 10.1002/pd.6639

By:

Ren, Jun;
Peng, Cuiting;
Chen, Han;
Zhou, Fan;
Keqie, Yuezhi;
Li, Yutong;
Yang, Hong;
Zhang, Haixia;
Du, Ze;
Hu, Ting;
Zhang, Xuemei;
Luo, Shan;
Fan, Wei;
Wang, Yan;
Wang, He;
Chen, Xinlian;
Liu, Shanling

Publication type:

Article

Idiopathic polyhydramnios and postnatal outcomes of children: The role of exome sequencing.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1279, doi. 10.1002/pd.6573

By:

Grausz, Noémie;
Senat, Marie‐Victoire;
Colmant, Claire;
Boizard, Anne;
Benachi, Alexandra;
Bouchghoul, Hanane

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1277, doi. 10.1002/pd.6379
Publication type:: Article