Works matching IS 01973851 AND DT 2006 AND VI 26 AND IP 8

Results: 27

Maternal serum ADAM12 levels in Down and Edwards' syndrome pregnancies at 9-12 weeks' gestation.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 689, doi. 10.1002/pd.1480

By:

Laigaard, Jennie;
Cuckle, Howard;
Wewer, Ulla M.;
Christiansen, Michael

Publication type:

Article

First- and second-trimester Down syndrome screening markers in pregnancies achieved through assisted reproductive technologies (ART): a FASTER trial study.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 672, doi. 10.1002/pd.1469

By:

Lambert-Messerlian, G.;
Dugoff, L.;
Vidaver, J.;
Canick, J. A.;
Malone, F. D.;
Ball, R. H.;
Comstock, C. H.;
Nyberg, D. A.;
Saade, G.;
Eddleman, K.;
Klugman, S.;
Craigo, S. D.;
Timor-Tritsch, I. E.;
Carr, S. R.;
Wolfe, H. M.;
D'Alton, M. E.

Publication type:

Article

Prenatal diagnosis of free sialic acid storage disorders (SASD).

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 655, doi. 10.1002/pd.1431

By:

Aula, Nina;
Aula, Pertti

Publication type:

Article

Prenatal Marfan syndrome: report of one case and review of the literature.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 696, doi. 10.1002/pd.1482

By:

Lopes, K. R. M.;
Delezoide, A. L.;
Baumann, C.;
Vuillard, E.;
Luton, D.;
Chitrit, Y.;
Azancot, A.

Publication type:

Article

Prenatal diagnostic indicators of paternal uniparental disomy 14.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 662, doi. 10.1002/pd.1453

By:

Curtis, Logos;
Antonelli, Eric;
Vial, Yvan;
Rimensberger, Peter;
Le Merrer, Martine;
Hinard, Christine;
Bottani, Armand;
Fokstuen, Siv

Publication type:

Article

Multi-centre first-trimester screening for Down syndrome in the Netherlands in routine clinical practice.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 711, doi. 10.1002/pd.1486

By:

Schielen, P. C. J. I.;
van Leeuwen-Spruijt, M.;
Belmouden, I.;
Elvers, L. H.;
Jonker, M.;
Loeber, J. G.

Publication type:

Article

Repeated measurement of pregnancy-associated plasma protein-A (PAPP-A) in Down syndrome screening: A validation study.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 730, doi. 10.1002/pd.1497

By:

Palomaki, Glenn E.;
Wright, David E.;
Summers, Anne M.;
Neveux, Louis M.;
Meier, Christian;
O'Donnell, Andrea;
Huang, Tianhua;
Knight, George J.;
Haddow, James E.

Publication type:

Article

First trimester diagnosis of sirenomelia.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 684, doi. 10.1002/pd.1479

By:

Van Keirsbilck, J.;
Cannie, M.;
Robrechts, C.;
de Ravel, T.;
Dymarkowski, S.;
Van den Bosch, T.;
Van Schoubroeck, D.

Publication type:

Article

Diagnosis and prognosis of fetuses with double outlet right ventricle.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 740, doi. 10.1002/pd.1500

By:

Kim, Nancy;
Friedberg, Mark K.;
Silverman, Norman H.

Publication type:

Article

Prenatal diagnosis of Freeman-Sheldon syndrome and usefulness of an ultrasound fetal lip width normogram.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 679, doi. 10.1002/pd.1470

By:

Vimercati, Antonella;
Scioscia, Marco;
Burattini, Maria Gabriella;
Pontrelli, Giovanni;
Selvaggi, Luigi E.

Publication type:

Article

Fetal abdomino-perineal lymphangioma: differential diagnosis and management.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 692, doi. 10.1002/pd.1481

By:

York, Douglas G.;
Wolfe, Honor;
von Allmen, Daniel

Publication type:

Article

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 725, doi. 10.1002/pd.1496

By:

Chen, Chih-Ping;
Lin, Shuan-Pei;
Wang, Tzu-Hao;
Chen, Yann-Jang;
Chen, Ming;
Wang, Wayseen

Publication type:

Article

Outcome of fetal cerebral posterior fossa anomalies.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 707, doi. 10.1002/pd.1485

By:

Long, Audrey;
Moran, Paul;
Robson, Stephen

Publication type:

Article

Second-trimester diagnosis of mucopolysaccharidosis type IV a presenting as hydrops fetalis.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 750, doi. 10.1002/pd.1467

By:

Colmant, Claire;
Picone, Olivier;
Froissart, Roseline;
Labrune, Philippe;
Senat, Marie-Victoire

Publication type:

Article

Double aneuploid mosaicism 45,X/46,XX/47,XX,+18 in a fetus with cerebral malformations.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 755, doi. 10.1002/pd.1489

By:

Picone, Olivier;
Hirt, Raphaël;
Brisset, Sophie;
Frydman, René;
Senat, Marie-Victoire;
Tachdjian, Gérard

Publication type:

Article

Prenatal diagnosis of absent right and persistent left superior vena cava.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 700, doi. 10.1002/pd.1483

By:

Pasquini, Lucia;
Belmar, Cristian;
Seale, Anna;
Gardiner, Helena M.

Publication type:

Article

Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter).

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 757, doi. 10.1002/pd.1491

By:

Chen, Chih-Ping;
Lin, Chyi-Chyang;
Chang, Tung-Yao;
Li, Yueh-Chun;
Hsieh, Lie-Jiau;
Lee, Chen-Chi;
Chen, Li-Feng;
Wang, Wayseen

Publication type:

Article

Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 667, doi. 10.1002/pd.1462

By:

Shaffer, Brian L.;
Caughey, Aaron B.;
Norton, Mary E.

Publication type:

Article

First-trimester examination of fetal nasal bone in the Chinese population.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 703, doi. 10.1002/pd.1484

By:

Chen, Min;
Lee, Chin Peng;
Tang, Rebecca;
Chan, Ben;
Ou, Chun Quan;
Tang, Mary Hoi Yin

Publication type:

Article

False-positive diagnosis of intrauterine herpes simplex type 1 infection using PCR.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 749, doi. 10.1002/pd.1466

By:

Incerti, Maddalena;
Ghidini, Alessandro

Publication type:

Article

Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2→qter).

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 752, doi. 10.1002/pd.1488

By:

Chen, Chih-Ping;
Wang, Tzu-Hao;
Chern, Schu-Rern;
Tzen, Chin-Yuan;
Hsu, Chin-Yuan;
Lee, Chen-Chi;
Chen, Li-Feng;
Ma, Chung-Chun;
Chen, Po-Tsang;
Wang, Wayseen

Publication type:

Article

Two independent rare events-a mutation in the RUNX2 gene and a de novo balanced translocation-in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 759, doi. 10.1002/pd.1499

By:

Caignec, Cédric Le;
Winer, Norbert;
Philippe, Henri-Jean;
Rival1, Jean-Marie

Publication type:

Article

Prenatal diagnosis may represent a point of entry of genetic science in sub-Saharan Africa: a survey on the attitudes of medical students and physicians from Cameroon.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 760, doi. 10.1002/pd.1502

By:

Wonkam, Ambroise;
Angwafo, Fru F

Publication type:

Article

Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot study.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 719, doi. 10.1002/pd.1490

By:

Giordano, P. C.;
Plancke, A.;
Van Meir, C. A.;
Janssen, C. A. H.;
Kok, P. J. M. J.;
Van Rooijen-Nijdam, I. H.;
Tanis, B. C.;
van Huisseling, J. C. M.;
Versteegh, F. G. A.

Publication type:

Article

Partial tetrasomy chromosome 14. A new prenatal diagnosis case.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 746, doi. 10.1002/pd.1465

By:

Fdez-Novoa, C.;
Vargas, M. T.;
Torres, F.;
Muñoz, J.

Publication type:

Article

Elevated maternal serum alpha-fetoprotein, umbilical vein varix, and mesenchymal dysplasia: are they related?

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 8, p. 659, doi. 10.1002/pd.1436

By:

Mulch, Amanda D.;
Stallings, Shawn P.;
Salafia, Carolyn M.

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2006, v. 26, n. 8, p. 762, doi. 10.1002/pd.1333
Publication type:: Article