Works matching IS 01973851 AND DT 2023 AND VI 43 AND IP 2

Results: 16

Prenatal screening and diagnosis of sex chromosome conditions: The new normal?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 131, doi. 10.1002/pd.6323

By:

Hui, Lisa;
Langlois, Sylvie

Publication type:

Article

Cover Image.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 1, doi. 10.1002/pd.6330

By:

Steffensen, Ellen Hollands;
Skakkebæk, Anne;
Gadsbøll, Kasper;
Petersen, Olav Bjørn;
Westover, Thomas;
Strange, Heather;
Vogel, Ida

Publication type:

Article

Prenatal ultrasound finding of atypical genitalia: Counseling, genetic testing and outcomes.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 162, doi. 10.1002/pd.6205

By:

van Bever, Yolande;
Groenenberg, Irene A. L.;
Knapen, Maarten F. C. M.;
Dessens, Arianne B.;
Hannema, Sabine E.;
Wolffenbuttel, Katja P.;
Diderich, Karin E. M.;
Hoefsloot, Lies H.;
Srebniak, Malgorzata I.;
Bruggenwirth, Hennie T.

Publication type:

Article

Prenatal phenotype of 47, XXY (Klinefelter syndrome).

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 207, doi. 10.1002/pd.6071

By:

Swanson, Kate;
Bishop, Juliet C.;
Al‐Kouatly, Huda B.;
Makhamreh, Mona;
Felton, Thomas;
Vora, Neeta L.;
Sparks, Teresa N.;
Jelin, Angie C.

Publication type:

Article

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 144, doi. 10.1002/pd.6322

By:

Steffensen, Ellen Hollands;
Skakkebæk, Anne;
Gadsbøll, Kasper;
Petersen, Olav Bjørn;
Westover, Thomas;
Strange, Heather;
Vogel, Ida

Publication type:

Article

State‐wide increase in prenatal diagnosis of klinefelter syndrome on amniocentesis and chorionic villus sampling: Impact of non‐invasive prenatal testing for sex chromosome conditions.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 156, doi. 10.1002/pd.6103

By:

Loughry, Lulu;
Pynaker, Cecilia;
White, Mary;
Halliday, Jane;
Hui, Lisa

Publication type:

Article

Multicenter clinical experience with non‐invasive cell‐free DNA screening for monosomy X and related X‐chromosome variants.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 192, doi. 10.1002/pd.6320

By:

Bedei, Ivonne;
Gehrke, Tascha;
Gloning, Karl‐Philipp;
Meyer‐Wittkopf, Matthias;
Willner, Daria;
Krapp, Martin;
Scharf, Alexander;
Degenhardt, Jan;
Heling, Kai‐Sven;
Kozlowski, Peter;
Trautmann, Kathrin;
Jahns, Kai M.;
Geipel, Annegret;
Baumüller, Jan‐Erik;
Wilhelm, Lucas;
Gottschalk, Ingo;
Schröer, Andreas;
Graf, Alexander;
Wolter, Aline;
Schenk, Johanna

Publication type:

Article

Performance of a cell‐free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low‐risk cell‐free DNA screening.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 213, doi. 10.1002/pd.6307

By:

Scarff, Katrina L.;
Flowers, Nicola;
Love, Clare J.;
Archibald, Alison D.;
Hunt, Clare E.;
Giouzeppos, Olivia;
Elliott, Justine;
Delatycki, Martin B.;
Pertile, Mark D.

Publication type:

Article

Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 183, doi. 10.1002/pd.6302

By:

Bedei, Ivonne;
Gloning, Karl‐Philipp;
Joyeux, Luc;
Meyer‐Wittkopf, Matthias;
Willner, Daria;
Krapp, Martin;
Scharf, Alexander;
Degenhardt, Jan;
Heling, Kai‐Sven;
Kozlowski, Peter;
Trautmann, Kathrin;
Jahns, Kai M.;
Geipel, Annegret;
Tekesin, Ismail;
Elsässer, Michael;
Wilhelm, Lucas;
Gottschalk, Ingo;
Baumüller, Jan‐Erik;
Birdir, Cahit;
Schröer, Andreas

Publication type:

Article

A systematic review and meta‐analysis of cell‐free DNA testing for detection of fetal sex chromosome aneuploidy.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 133, doi. 10.1002/pd.6298

By:

Shear, Matthew A.;
Swanson, Kate;
Garg, Ria;
Jelin, Angie C.;
Boscardin, John;
Norton, Mary E.;
Sparks, Teresa N.

Publication type:

Article

Reproductive health in Turner syndrome: A narrative review.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 261, doi. 10.1002/pd.6261

By:

Whigham, Carole‐Anne;
Vollenhoven, Beverley;
Vincent, Amanda J.

Publication type:

Article

Prenatal diagnosis of sex chromosome aneuploidy—What do we tell the prospective parents?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 250, doi. 10.1002/pd.6256

By:

Reimers, Rebecca;
High, Frances;
Kremen, Jessica;
Wilkins‐Haug, Louise

Publication type:

Article

Klinefelter Syndrome: What should we tell prospective parents?

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 240, doi. 10.1002/pd.6250

By:

White, Mary;
Zacharin, Margaret R.;
Fawcett, Susan;
McGillivray, George

Publication type:

Article

When a sex chromosome aneuploidy is diagnosed—views from a parent support organisation.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 235, doi. 10.1002/pd.6222

By:

Fisher, Jane;
McInnes‐Dean, Hannah

Publication type:

Article

Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 2, p. 226, doi. 10.1002/pd.6217

By:

Johnston, Molly;
Warton, Chanelle;
Pertile, Mark D.;
Taylor‐Sands, Michelle;
Delatycki, Martin B.;
Hui, Lisa;
Savulescu, Julian;
Mills, Catherine

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2023, v. 43, n. 2, p. 129, doi. 10.1002/pd.6174
Publication type:: Article