Works matching IS 01973851 AND DT 2003 AND VI 23 AND IP 6

Results: 20

Prenatal diagnosis of DandyWalker syndrome in early pregnancy presenting with increased nuchal translucency and generalized edema at 13 weeks of gestation.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 514, doi. 10.1002/pd.610

By:

Sheng Hsien Chen;
Mike Yan-Sheng Lin;
Fong-Ming Chang

Publication type:

Article

Prenatal diagnosis of limbbody wall complex in early pregnancy using three-dimensional ultrasound.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 513, doi. 10.1002/pd.609

By:

I-Feng Liu;
Chen-Hsiang Yu;
Chiung-Hsing Chang;
Fong-Ming Chang

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2003, v. 23, n. 6, p. 522, doi. 10.1002/pd.530
Publication type:: Article

Prenatal management of mosaic tetrasomy 5p. K. S. Reddy and B. Huang. Prenatal Diagnosis 2003; 1: 8285.

Published in:: Prenatal Diagnosis, 2003, v. 23, n. 6, p. 521, doi. 10.1002/pd.661
Publication type:: Article

The influence of IVF, multiple gestation and miscarriage on the acceptance of genetic amniocentesis.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 501, doi. 10.1002/pd.633

By:

Andrew Elimian;
Marcy Demsky;
Reinaldo Figueroa;
Paul Ogburn;
Alan R. Spitzer;
J. Gerald Quirk

Publication type:

Article

Prenatal diagnosis of congenital rubella infection in the second trimester of pregnancy.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 509, doi. 10.1002/pd.631

By:

Julian W. Tang;
Emma Aarons;
Louise M. Hesketh;
S. Strobel;
Gunnar Schalasta;
Eric Jauniaux;
Nicola S. Brink;
Gisela Enders

Publication type:

Article

Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 504, doi. 10.1002/pd.629

By:

Chih-Ping Chen;
Shuan-Pei Lin;
Schu-Rern Chern;
Shin-Lin Shih;
Chen-Chi Lee;
Wayseen Wang;
You-Wei Liao

Publication type:

Article

Absence of fetal nasal bone and aneuploidies at first-trimester nuchal translucency screening in unselected pregnancies.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 496, doi. 10.1002/pd.628

By:

Maria Angelica Zoppi;
Rosa Maria Ibba;
Carolina Axiana;
Marcella Floris;
Fabiola Manca;
Giovanni Monni

Publication type:

Article

Amniotic fluid human chorionic gonadotrophin and alpha-fetoprotein levels in pregnancies conceived after assisted reproduction.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 484, doi. 10.1002/pd.625

By:

P. W. Hui;
Y. H. Lam;
M. H. Y. Tang;
E. H. Y. Ng;
W. S. B. Yeung;
P. C. Ho

Publication type:

Article

Sirenomelia, the mermaid syndromedetection in the first trimester.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 493, doi. 10.1002/pd.624

By:

Monika Schiesser;
Wolfgang Holzgreve;
Olav Lapaire;
Nils Willi;
Hans Lüthi;
Roberto Lopez;
Sevgi Tercanli

Publication type:

Article

A classification of pregnancy losses after invasive prenatal diagnostic procedures: an approach to allow comparison of units with a different case mix.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 488, doi. 10.1002/pd.623

By:

Rashmi Nanal;
Phillipa Kyle;
Peter W. Soothill

Publication type:

Article

Association of partial trisomy 9 (9pter→q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts, and ventriculomegaly.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 519, doi. 10.1002/pd.622

By:

Chih-Ping Chen;
Chyong-Hsin Hsu;
Shuan-Pei Lin;
Che-Sheng Ho;
Chen-Chi Lee;
Wayseen Wang

Publication type:

Article

Prenatal diagnosis of de novo partial trisomy Xq (Xq22.1→qter) and terminal Xp deletion following sonographic detection of intrauterine growth restriction.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 518, doi. 10.1002/pd.621

By:

Chih-Ping Chen

Publication type:

Article

Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 461, doi. 10.1002/pd.620

By:

Sophie Brisset;
Azzedine Aboura;
François Audibert;
Jean-Marc Costa;
Aurore Coulomb L'Herminé;
Valérie Gautier;
René Frydman;
Gérard Tachdjian

Publication type:

Article

Prenatal diagnosis for Epidermolysis bullosa: a study of 144 consecutive pregnancies at risk.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 447, doi. 10.1002/pd.619

By:

Ellen G. Pfendner;
Aoi Nakano;
Leena Pulkkinen;
Angela M. Christiano;
Jouni Uitto

Publication type:

Article

Cystic fibrosis: selecting the prenatal screening strategy of choice.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 474, doi. 10.1002/pd.618

By:

N. J. Wald;
J. K. Morris;
C. H. Rodeck;
J. E. Haddow;
G. E. Palomaki

Publication type:

Article

Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 457, doi. 10.1002/pd.617

By:

Rodney Camire;
Ruth Ann Denchy;
George A. Day;
Patricia Lanzano;
Sujit Sheth;
Stephen Brown

Publication type:

Article

Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 515, doi. 10.1002/pd.615

By:

Chih-Ping Chen;
Jin-Chung Shih;
Jui-Hsing Chang;
Yi-Hui Lin;
Wayseen Wang

Publication type:

Article

Accuracy of trisomy 18 screening using the second-trimester triple test.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 443, doi. 10.1002/pd.614

By:

Chris Meier;
Tianhua Huang;
Philip R. Wyatt;
Anne M. Summers

Publication type:

Article

Early vaginal bleeding and first-trimester markers for Down syndrome.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 6, p. 470, doi. 10.1002/pd.611

By:

Pierangela De Biasio;
Silvana Canini;
Angela Crovo;
Federico Prefumo;
Pier Luigi Venturini

Publication type:

Article