Works matching IS 01973851 AND DT 2005 AND VI 25 AND IP 11

Results: 26

Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter).

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1069, doi. 10.1002/pd.1298

By:

Chen, Chih-Ping;
Chern, Schu-Rern;
Chang, Tung-Yao;
Lee, Chen-Chi;
Chen, Wen-Lin;
Wang, Wayseen

Publication type:

Article

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA).

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1032, doi. 10.1002/pd.1247

By:

Hochstenbach, R.;
Meijer, J.;
van de Brug, J.;
Vossebeld-Hoff, I.;
Jansen, R.;
van der Luijt, R. B.;
Sinke, R. J.;
Page-Christiaens, G. C. M. L.;
Ploos van Amstel, J.-K.;
de Pater, J. M.

Publication type:

Article

Is there an increased rate of anencephaly in twins?

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1007, doi. 10.1002/pd.1233

By:

Ben-Ami, Ido;
Vaknin, Zvika;
Reish, Orit;
Sherman, Dan;
Herman, Arie;
Maymon, Ron

Publication type:

Article

Hypospadias in sons of women exposed to ditheylstilbestrol: a true trans-generational effect?

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1072, doi. 10.1002/pd.1289

By:

Jouannic, J. M.;
Bénifla, J. L.

Publication type:

Article

Early ultrasonographic changes in Fowler syndrome features and review of the literature.

Published in:

2005

By:

Usta, Ihab M.;
AbuMusa, Antoine A.;
Khoury, Nabil G.;
Nassar, Anwar H.

Publication type:

journal article

Gorlin syndrome presenting as prenatal chylothorax in a girl.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 997, doi. 10.1002/pd.1231

By:

Geneviève, D.;
Walter, E.;
Gorry, P.;
Jacquemont, M. L.;
Dupic, L.;
Layet, V.;
Munnich, A.;
Cormier-Daire, V.;
Dommergues, M.;
Lyonnet, S.;
Mitanchez, D.

Publication type:

Article

Prenatal diagnosis of cyclopia and proboscis in a fetus with normal chromosome at 13 weeks of gestation by three-dimensional transabdominal sonography.

Published in:

2005

By:

Cho, Fu-Nan;
Kan, Yuen-Yee;
Chen, San-Nung;
Lee, Te-Ching;
Hsu, Ti-Ju;
Hsu, Pei-Hua

Publication type:

Case Study

TORCH test for fetal medicine indications: only CMV is necessary in the United Kingdom.

Published in:

2005

By:

Abdel-Fattah, Sherif A.;
Bhat, Abha;
Illanes, Sebastian;
Bartha, Jose L.;
Carrington, David

Publication type:

journal article

Congenital pulmonary myofibroblastic tumor--pathology and prenatal sonographic appearance.

Published in:

2005

By:

Reiss, Ari;
Goldberg, Yael;
Monichor, Mariana;
Drugan, Arie

Publication type:

Case Study

Population screening for fetal trisomy 21: easy access to screening should be balanced against a uniform ultrasound protocol.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 984, doi. 10.1002/pd.1217

By:

Gyselaers, Wilfried J. A.;
Vereecken, Annie J.;
Van Herck, Erik J. H.;
Straetmans, Dany P. L.;
de Jonge, Eric T. M.;
Ombelet, Willem U. A. M.;
Nijhuis, Jan G.

Publication type:

Article

Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1067, doi. 10.1002/pd.1297

By:

Chen, Chih-Ping;
Chern, Schu-Rern;
Chen, Li-Feng;
Chen, Wen-Lin;
Wang, Wayseen

Publication type:

Article

Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1024, doi. 10.1002/pd.1241

By:

Aslan, Halil;
Karaman, Birsen;
Yildirim, Gokhan;
Ceylan, Yavuz

Publication type:

Article

Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1011, doi. 10.1002/pd.1238

By:

Percesepe, Antonio;
Ferrari, Maurizio;
Coviello, Domenico;
Zanussi, Monica;
Castagni, Marina;
Neri, Isabella;
Travi, Maurizio;
Forabosco, Antonino;
Tedeschi, Silvana

Publication type:

Article

Prenatal diagnosis of cystinosis by quantitative measurement of cystine in chorionic villi and cultured cells.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1045, doi. 10.1002/pd.1249

By:

Jackson, Marie;
Young, Elisabeth

Publication type:

Article

Reliable test for prenatal prediction of fetal RhD type using maternal plasma from RhD negative women.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1040, doi. 10.1002/pd.1248

By:

Clausen, Frederik Banch;
Krog, Grethe Risum;
Rieneck, Klaus;
Nielsen, Leif Kofoed;
Lundquist, Rasmus;
Finning, Kirstin;
Dickmeiss, Ebbe;
Hedegaard, Morten;
Dziegiel, Morten Hanefeld

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1073, doi. 10.1002/pd.1025
Publication type:: Article

Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1015, doi. 10.1002/pd.1237

By:

Daniel-Spiegel, Etty;
Ghalamkarpour, Arash;
Spiegel, Ronen;
Weiner, Ehud;
Vikkula, Miikka;
Shalev, Eliezer;
Shalev, Stavit Alon

Publication type:

Article

Y chromosome heterochromatin variation detected at prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1062, doi. 10.1002/pd.1280

By:

Cotter, Philip D.;
Norton, Mary E.

Publication type:

Article

Maternal serum biochemistry at 11-13(+6) weeks in relation to the presence or absence of the fetal nasal bone on ultrasonography in chromosomally abnormal fetuses: an updated analysis of integrated ultrasound and biochemical screening.

Published in:

2005

By:

Cicero, Simona;
Spencer, Kevin;
Avgidou, Kyriaki;
Faiola, Stefano;
Nicolaides, Kypros H.

Publication type:

journal article

Increasing detection rates of birth defects by prenatal ultrasound leading to apparent increasing prevalence. Lessons learned from the population-based registry of birth defects of Barcelona.

Published in:

2005

By:

Salvador, Joaquín;
Borrell, Antoni;
Lladonosa, Anna;
Salvador, Joaquín

Publication type:

journal article

Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1048, doi. 10.1002/pd.1255

By:

Surti, Urvashi;
Hill, Lyndon M.;
Dunn, Jeanette;
Prosen, Tracy;
Hoffner, Lori

Publication type:

Article

Sonographic diagnosis of fetal adrenal hyperplasia: utility for prenatal corticotherapy.

Published in:

2005

By:

Cassart, Marie;
Massez, Anne;
Donner, Catherine;
Heinrichs, Claudine;
Avni, Freddy

Publication type:

Case Study

The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis.

Published in:

2005

By:

Milunsky, A.;
Konialis, C.;
Shim, S. H.;
Maher, T. A.;
Spengos, K.;
Ito, M.;
Pangalos, C.

Publication type:

journal article

Three-dimensional ultrasound of dicephalus conjoined twins at 9 weeks of gestation.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1063, doi. 10.1002/pd.1283

By:

Suzumori, Nobuhiro;
Nakanishi, Tamao;
Kaneko, Saori;
Yamamoto, Tamao;
Tanemura, Mitsuyo;
Suzuki, Yoshikatsu;
Suzumori, Kaoru

Publication type:

Article

Sterol profiling of amniotic fluid: a routine method for the detection of distal cholesterol synthesis deficit.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1000, doi. 10.1002/pd.1254

By:

Chevy, F.;
Humbert, L.;
Wolf, C.

Publication type:

Article

Apert syndrome associated with increased fetal nuchal translucency.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 11, p. 1066, doi. 10.1002/pd.1294

By:

Aleem, S.;
Howarth, E. S.

Publication type:

Article