Works matching IS 01973851 AND DT 2023 AND VI 43 AND IP 6

Results: 16

Likely pathogenic variant in the BICD2 gene in fetus presenting with non‐immune hydrops.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 727, doi. 10.1002/pd.6386

By:

Chandler, Natalie;
Brace, Poppy;
Roberts, Rowenna;
Mellis, Rhiannon

Publication type:

Article

Abnormalities of the corpus callosum. Can prenatal imaging predict the genetic status? Correlations between imaging phenotype and genotype.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 746, doi. 10.1002/pd.6382

By:

Nguyen, Toan;
Heide, Solveig;
Guilbaud, Lucie;
Valence, Stéphanie;
Perre, Saskia Vande;
Blondiaux, Eléonore;
Keren, Boris;
Quenum‐Miraillet, Geneviève;
Jouannic, Jean‐Marie;
Mandelbrot, Laurent;
Picone, Olivier;
Guet, Agnès;
Tsatsaris, Vassilis;
Milh, Mathieu;
Girard, Nadine;
Vincent, Marie;
Nizon, Mathilde;
Poirsier, Céline;
Vivanti, Alexandre;
Benachi, Alexandra

Publication type:

Article

Maternally inherited autosomal dominant PLAG‐1 related Silver Russell syndrome in a fetus with intra‐uterine growth restriction.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 724, doi. 10.1002/pd.6364

By:

Tse, Wing Ting;
Bass, Charlotte;
Gurney, Leo;
Kinning, Esther

Publication type:

Article

The value and limitations of using predetermined criteria in decision making for maternal‐fetal interventions.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 792, doi. 10.1002/pd.6363

By:

Premkumar, Ashish;
Fry, Jessica T.;
Bolden, Janelle R.;
Grobman, William A.;
Michelson, Kelly N.

Publication type:

Article

Early and severe tricuspid valve dysplasia in a fetus with cardiospondylocarpofacial syndrome due to a variant c.616T>G p.(Tyr206Asp) in MAP3K7.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 721, doi. 10.1002/pd.6358

By:

Vasishta, Subrahmanya;
Teli, Akkatai S.;
Vasudeva, Akhila;
Girisha, Katta M.;
Nayak, Shalini S.

Publication type:

Article

Pregnancy termination at a viable stage in daily clinical practice: A nationwide mortality follow‐back study in Flanders, Belgium.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 781, doi. 10.1002/pd.6356

By:

Roets, Ellen;
Beernaert, Kim;
Chambaere, Kenneth;
Deliens, Luc;
van Berkel, Kim;
De Catte, Luc;
Vanhaesebrouck, Sophie;
Roelens, Kristien;
Dombrecht, Laure

Publication type:

Article

Fetal hydrops caused by a novel pathogenic MECOM variant.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 717, doi. 10.1002/pd.6353

By:

Wall, Elizabeth;
Forsyth, Joan;
Kinning, Esther;
Marton, Tamás

Publication type:

Article

Reply to: Addressing expectations of therapeutic options for children with hydrocephalus—A comment on "Fetal Cerebral Ventriculomegaly. What do we tell the prospective parents?".

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 806, doi. 10.1002/pd.6350

By:

Giorgione, Veronica;
Haratz, Karina Krajden;
Constantini, Shlomi;
Birnbaum, Roee;
Malinger, Gustavo

Publication type:

Article

X‐linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 730, doi. 10.1002/pd.6349

By:

Tanner, Laura M.;
Tynninen, Olli;
Piippo, Kirsi;
Puhakka, Antti M.

Publication type:

Article

Investigation into the genetics of fetal congenital lymphatic anomalies.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 703, doi. 10.1002/pd.6345

By:

Rogerson, Daniella;
Alkelai, Anna;
Giordano, Jessica;
Pantrangi, Madhulatha;
Hsiao, Meng‐Chang;
Nhan‐Chang, Chia‐Ling;
Motelow, Joshua E.;
Aggarwal, Vimla;
Goldstein, David;
Wapner, Ron;
Shawber, Carrie J.

Publication type:

Article

Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcome.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 756, doi. 10.1002/pd.6344

By:

Ashwal, Eran;
Blaser, Susan;
Leckie, Ashley;
Kajal, Dilkash;
Krishnan, Pradeep;
Chong, Karen;
Roifman, Maian;
Toi, Ants;
Chitayat, David

Publication type:

Article

Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 734, doi. 10.1002/pd.6340

By:

Courdier, Cécile;
Boudjarane, John;
Malan, Valérie;
Muti, Christine;
Sperelakis‐Beedham, Brian;
Odent, Sylvie;
Jaillard, Sylvie;
Quelin, Chloé;
Le Caignec, Cédric;
Patat, Olivier;
Dubucs, Charlotte;
Julia, Sophie;
Schluth‐Bolard, Caroline;
Goumy, Carole;
Redon, Sylvia;
Gaillard, Jean‐Baptiste;
Huynh, Minh Tuan;
Dupont, Céline;
Tabet, Anne‐Claude;
Cogan, Guillaume

Publication type:

Article

Receiving uncertain results from prenatal chromosomal microarray analysis: Women's decisions on continuation or termination of pregnancy.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 773, doi. 10.1002/pd.6337

By:

Libman, Vitalia;
Friedlander, Yechiel;
Chalk, Michal;
Hochner, Hagit;
Shkedi‐Rafid, Shiri

Publication type:

Article

Fetal agenesis of the septum pellucidum: Ultrasonic diagnosis and clinical significance.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 763, doi. 10.1002/pd.6316

By:

Hu, Xueyi;
Shang, Ning

Publication type:

Article

Fetal arthrogryposis—what do we tell the prospective parents?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 6, p. 798, doi. 10.1002/pd.6299

By:

Filges, Isabel;
Jünemann, Stephanie;
Viehweger, Elke;
Tercanli, Sevgi

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 6, p. 701, doi. 10.1002/pd.6178
Publication type:: Article