Works matching IS 01973851 AND DT 2022 AND VI 42 AND IP 5

Results: 15

Sonographic evaluation of umbilical cord thickness in monochorionic diamniotic twin pregnancies.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 636, doi. 10.1002/pd.6141

By:

Nunes, Clarissa Moraes;
Biancolin, Sckarlet Ernandes;
Miyadahira, Mariana Yumi;
Peres, Stela Verzinhasse;
de Carvalho, Mario Henrique Burlacchini;
Francisco, Rossana Pulcineli Vieira;
Brizot, Maria de Lourdes

Publication type:

Article

First trimester ultrasound in the age of cell‐free DNA screening: What are we missing?

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 542, doi. 10.1002/pd.6139

By:

Ramdaney, Aarti;
Mulligan, Shannon;
Wittman, Theresa;
Wagner, Chelsea

Publication type:

Article

Raine syndrome: Report of a novel mutation and review of the different antenatal imaging modalities used to diagnose this disease.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 589, doi. 10.1002/pd.6138

By:

Rameh, Georges;
Megarbane, Andre;
Jalbout, Liliane;
Snaifer, Elie;
Saliba, Souha;
Nassar, Anwar;
Chalouhi, Gihad

Publication type:

Article

Noninvasive prenatal testing of hereditary colorectal cancer syndromes using cell‐free DNA in maternal plasma.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 557, doi. 10.1002/pd.6137

By:

Wang, Yao;
Li, Suqing;
Wu, Di;
Yan, Hongli

Publication type:

Article

The Unethical Texas Heartbeat Law.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 535, doi. 10.1002/pd.6136

By:

Haining, Casey Michelle;
Keogh, Louise Anne;
Savulescu, Julian

Publication type:

Article

Fetal and neonatal abnormalities due to congenital syphilis: A literature review.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 643, doi. 10.1002/pd.6135

By:

David, Marion;
Hcini, Najeh;
Mandelbrot, Laurent;
Sibiude, Jeanne;
Picone, Olivier

Publication type:

Article

Prenatal bone abnormalities in three cases of familial hypocalciuric hypercalcemia.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 583, doi. 10.1002/pd.6134

By:

Frerot, Alice;
Baudouin, Véronique;
Rideau‐Batista, Aline;
Couderc, Anne;
Garel, Catherine;
Soltane, Samia;
Colella, Marina;
Vargas‐Poussou, Rosa;
Hureaux, Marguerite

Publication type:

Article

Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 574, doi. 10.1002/pd.6133

By:

Lamouroux, Audrey;
Dauge, Coralie;
Wells, Constance;
Mousty, Eve;
Pinson, Lucile;
Cavé, Hélène;
Capri, Yline;
Faure, Jean‐Michel;
Grosjean, Frédéric;
Sauvestre, Fanny;
Attié‐Bitach, Tania;
Pelluard, Fanny;
Geneviève, David

Publication type:

Article

Implementation of non‐invasive prenatal testing within a national UK antenatal screening programme: Impact on women's choices.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 549, doi. 10.1002/pd.6131

By:

Bowden, Bethan;
de Souza, Sikha;
Puchades, Alice;
Williams, Kindry;
Morgan, Sian;
Anderson, Sarah;
Tucker, David;
Hillier, Sharon

Publication type:

Article

Alobar holoprosencephaly: Exploring mothers' perspectives on prenatal decision‐making and prognostication.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 617, doi. 10.1002/pd.6130

By:

Elfarawi, Hunaydah;
Tolusso, Leandra;
McGowan, Michelle L.;
Cortezzo, DonnaMaria;
Vawter‐Lee, Marissa

Publication type:

Article

Motion corrected fetal body magnetic resonance imaging provides reliable 3D lung volumes in normal and abnormal fetuses.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 628, doi. 10.1002/pd.6129

By:

Davidson, Joseph;
Uus, Alena;
Egloff, Alexia;
van Poppel, Milou;
Matthew, Jacqueline;
Steinweg, Johannes;
Deprez, Maria;
Aertsen, Michael;
Deprest, Jan;
Rutherford, Mary

Publication type:

Article

COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 601, doi. 10.1002/pd.6113

By:

Coste, Thibault;
Vincent‐Delorme, Catherine;
Stichelbout, Morgane;
Devisme, Louise;
Gelot, Antoinette;
Deryabin, Igor;
Pelluard, Fanny;
Aloui, Chaker;
Leutenegger, Anne‐Louise;
Jouannic, Jean‐Marie;
Héron, Delphine;
Gould, Douglas B;
Tournier‐Lasserve, Elisabeth

Publication type:

Article

Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 611, doi. 10.1002/pd.6109

By:

Swanson, Kate;
Loeliger, Kelsey B.;
Chetty, Shilpa P.;
Sparks, Teresa N.;
Norton, Mary E.

Publication type:

Article

Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 5, p. 567, doi. 10.1002/pd.6009

By:

Filer, Dayne L.;
Mieczkowski, Piotr A.;
Brandt, Alicia;
Gilmore, Kelly L.;
Powell, Bradford C.;
Berg, Jonathan S.;
Wilhelmsen, Kirk C.;
Vora, Neeta L.

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2022, v. 42, n. 5, p. 533, doi. 10.1002/pd.5962
Publication type:: Article