Works matching IS 01973851 AND DT 2010 AND VI 30 AND IP 3

Results: 20

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2010, v. 30, n. 3, p. i, doi. 10.1002/pd.2355
Publication type:: Article

Hematological characteristics in neonates with twin anemia-polycythemia sequence (TAPS).

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 251, doi. 10.1002/pd.2453

By:

Lopriore, E.;
Slaghekke, F.;
Oepkes, D.;
Middeldorp, J. M.;
Vandenbussche, F. P. H. A.;
Walther, F. J.

Publication type:

Article

Hematological characteristics in neonates with twin anemia-polycythemia sequence (TAPS)

Published in:

2010

By:

Lopriore E;
Slaghekke F;
Oepkes D;
Middeldorp JM;
Vandenbussche FP;
Walther FJ

Publication type:

Journal Article

Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 216, doi. 10.1002/pd.2440

By:

Poon, Leona C. Y.;
Stratieva, Violeta;
Piras, Silvia;
Piri, Solmaz;
Nicolaides, Kypros H.

Publication type:

Article

First-trimester sonographic findings in trisomy 18: a review of 53 cases.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 256, doi. 10.1002/pd.2462

By:

Sepulveda, Waldo;
Wong, Amy E.;
Dezerega, Victor

Publication type:

Article

Maternal plasma soluble fms-like tyrosine kinase-1 and free vascular endothelial growth factor at 11 to 13 weeks of gestation in preeclampsia.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 191, doi. 10.1002/pd.2433

By:

Akolekar, Ranjit;
de Cruz, Jader;
Foidart, Jean-Michel;
Munaut, Carine;
Nicolaides, Kypros H.

Publication type:

Article

Pre- and postnatal diagnosis and outcome of fetuses and neonates with esophageal atresia and tracheoesophageal fistula.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 274, doi. 10.1002/pd.2466

By:

de Jong, E. M.;
de Haan, M. A. M;
Gischler, S. J.;
Hop, W.;
Cohen-Overbeek, T. E.;
Bax, N. M. A.;
de Klein, A.;
Tibboel, D.;
Grijseels, E. W. M.

Publication type:

Article

Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 207, doi. 10.1002/pd.2437

By:

Malcov, Mira;
Reches, Adi;
Ben-Yosef, Dalit;
Cohen, Tania;
Amit, Ami;
Dgany, Orly;
Tamary, Hannah;
Yaron, Yuval

Publication type:

Article

Difference in nuchal translucency between monozygotic and dizygotic spontaneously conceived twins.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 247, doi. 10.1002/pd.2450

By:

Cheng, Po-Jen;
Huang, Shang-Yu;
Shaw, Sheng-Wen;
Hsiao, Ching-Hwa;
Kao, Chuan-Chi;
Chueh, Ho-Yen;
Hsieh, T'sang-T'ang

Publication type:

Article

Identification of circulating placental mRNA in maternal blood of pregnancies affected with fetal congenital heart diseases at the second trimester of pregnancy: implications for early molecular screening.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 229, doi. 10.1002/pd.2443

By:

Arcelli, Diego;
Farina, Antonio;
Cappuzzello, Claudia;
Bresin, Antonella;
De Sanctis, Paola;
Perolo, Antonella;
Prandstraller, Daniela;
Valentini, Davide;
Zucchini, Cinzia;
Priori, Silvia;
Rizzo, Nicola

Publication type:

Article

Effect of religion on the attitude of primiparous women toward genetic testing.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 241, doi. 10.1002/pd.2447

By:

Usta, Ihab M.;
Nassar, Anwar H.;
Abu-Musa, Antoine A.;
Hannoun, Antoine

Publication type:

Article

Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 284, doi. 10.1002/pd.2458

By:

Houweling, A. C.;
de Mooij, Y. M.;
van der Burgt, I.;
Yntema, H. G.;
Lachmeijer, A. M. A.;
Go, A. T. J. I.

Publication type:

Article

Fetal anatomic survey using three-dimensional ultrasound in conjunction with first-trimester nuchal translucency screening.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 267, doi. 10.1002/pd.2446

By:

Bhaduri, Mousumi;
Fong, Katherine;
Toi, Ants;
Tomlinson, George;
Okun, Nan

Publication type:

Article

Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 280, doi. 10.1002/pd.2439

By:

Malvestiti, Francesca;
De Toffol, Simona;
Chinetti, Sara;
Grimi, Beatrice;
Favero, Giancarlo;
Borsatti, Alessandro;
Maggi, Federico;
Simoni, Giuseppe;
Grati, Francesca Romana

Publication type:

Article

Maternal plasma levels of follistatin-related gene protein in the first trimester of pregnancies with Down syndrome.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 224, doi. 10.1002/pd.2441

By:

Miron, Pierre;
Lambert, Jean;
Marcil, Anne;
Cowans, Nicholas J.;
Stamatopoulou, Anastasia;
Spencer, Kevin

Publication type:

Article

Non-invasive detection and quantification of human foetal brain lactate in utero by magnetic resonance spectroscopy.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 260, doi. 10.1002/pd.2463

By:

Charles-Edwards, Geoffrey D.;
Jan, Wajanat;
To, Meekai;
Maxwell, Darryl;
Keevil, Stephen F.;
Robinson, Richard

Publication type:

Article

Trends in prenatal screening and diagnostic testing among women referred for advanced maternal age.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 198, doi. 10.1002/pd.2434

By:

Nakata, Naomi;
Wang, Yuemei;
Bhatt, Sucheta

Publication type:

Article

First trimester aneuploidy screening in the presence of a vanishing twin: implications for maternal serum markers.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 235, doi. 10.1002/pd.2445

By:

Spencer, K.;
Staboulidou, I.;
Nicolaides, K. H.

Publication type:

Article

Trisomy 18 and 13 screening: consequences for the Dutch Down syndrome screening programme.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 287, doi. 10.1002/pd.2467

By:

Koster, M. P. H.;
Stoutenbeek, P.;
Visser, G. H. A.;
Schielen, P. C. J. I.

Publication type:

Article

Maternal serum human placental growth hormone at 11 to 13 weeks in trisomy 21 and trisomy 18 pregnancies.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 3, p. 212, doi. 10.1002/pd.2438

By:

Sifakis, Stavros;
Akolekar, Ranjit;
Syngelaki, Argyro;
De Cruz, Jader;
Nicolaides, Kypros H

Publication type:

Article