Works matching IS 01973851 AND DT 2006 AND VI 26 AND IP 12

Results: 19

Chorionic villus sampling for beta-thalassemia: the first report of experience in Iran.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1131, doi. 10.1002/pd.1572

By:

Akhlaghpoor, Shahram

Publication type:

Article

Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1168, doi. 10.1002/pd.1583

By:

Aguinaga, M.;
Razo, G.;
Castro, J.;
Mayén-Molina, D. G.

Publication type:

Article

A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1151, doi. 10.1002/pd.1576

By:

Colombani, Marina;
Laurent, Nicole;
Le Merrer, Martine;
Delezoide, Anne-Lise;
Thauvin-Robinet, Christel;
Huet, Frédéric;
Sagot, Paul;
Couvreur, Stéphanie;
Rousseau, Thierry;
Robertson, Stephen P.;
Faivre, Laurence

Publication type:

Article

Limited value of echography to predict true fetal mosaicism for trisomy 12.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1186, doi. 10.1002/pd.1587

By:

Gentilin, Barbara;
Giardino, Daniela;
Boschetto, Chiara;
Guerneri, Silvana;
Fortuna, Renato;
Rizzuti, Tommaso;
Lalatta, Faustina

Publication type:

Article

Prenatal diagnosis of neurofibromatosis type 1: sonographic and MRI findings.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1110, doi. 10.1002/pd.1560

By:

McEwing, Rachael L.;
Joelle, Roume;
Mohlo, Marc;
Bernard, Jean-Pierre;
Hillion, Yvette;
Ville, Yves

Publication type:

Article

Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1160, doi. 10.1002/pd.1582

By:

Allen, S. K.;
Luharia, A.;
Gould, C. P.;
MacDonald, F.;
Larkins, S.;
Davison, E. V.

Publication type:

Article

Prenatal sonographic diagnosis of Malpuech syndrome.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1121, doi. 10.1002/pd.1564

By:

Turnbull, Clare;
Lees, Melissa;
Chitty, Lyn S

Publication type:

Article

Supernumerary marker chromosomes detected in 100 000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1142, doi. 10.1002/pd.1575

By:

Huang, Bing;
Solomon, Sharon;
Thangavelu, Maya;
Peters, Katherine;
Bhatt, Sucheta

Publication type:

Article

De novo chromosomal abnormalities and month of conception. Data from the southern hemisphere.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1184, doi. 10.1002/pd.1586

By:

Gadow, Enrique;
Petracchi, Florencia;
Poletta, Fernando A.;
Castilla, Eduardo E.

Publication type:

Article

Single large study or meta-analysis parameters: choosing the most appropriate tool for Down syndrome screening in the first trimester.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1124, doi. 10.1002/pd.1568

By:

Ramos-Corpas, Domingo;
Santiago, Juan C.

Publication type:

Article

Three stage contingent screening for Down syndrome.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1183, doi. 10.1002/pd.1579

By:

Huttly, Wayne J.;
Morris, Joan K.;
Bestwick, Jonathan P;
Wald, Nicholas J.;
Murphy, Karl;
Pandya, Pranav P.

Publication type:

Article

The 'Consecutive Combined Test'-using Double test from week 8 + 0 and Nuchal Translucency Scan, for first trimester screening for Down Syndrome.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1105, doi. 10.1002/pd.1487

By:

Schiøtt, Kirsten Marie;
Christiansen, Michael;
Petersen, Olav Bjørn;
Sørensen, Tina Lind;
Uldbjerg, Niels

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1190, doi. 10.1002/pd.1337
Publication type:: Article

First-trimester maternal dried blood Down syndrome screening marker levels in early pregnancy loss.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1137, doi. 10.1002/pd.1574

By:

Krantz, David;
Hallahan, Terrence;
Ishack, Stephanie;
Macri, V. James;
Macri, James N.

Publication type:

Article

Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1179, doi. 10.1002/pd.1585

By:

Moradkhani, Kamran;
Puechberty, Jacques;
Blanchet, Patricia;
Coubes, Christine;
Lallaoui, Hakima;
Lewin, Patricia;
Lefort, Genevieve;
Sarda, Pierre

Publication type:

Article

A matter of opinion of evidence!

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1184, doi. 10.1002/pd.1578

By:

Wright, Dave;
Bradbury, Ian;
Cuckle, Howard;
Gardosi, Jason;
Tonks, Ann;
Standing, Sue;
Benn, Peter

Publication type:

Article

Quantitative distribution of a panel of circulating mRNA in preeclampsia versus controls.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1115, doi. 10.1002/pd.1562

By:

Farina, Antonio;
Sekizawa, Akihiko;
Purwosunu, Yuditiya;
Rizzo, Nicola;
Banzola, Irina;
Concu, Manuela;
Morano, Danila;
Giommi, Federica;
Bevini, Maurizio;
Mabrook, Mohamad;
Carinci, Paolo;
Okai, Takashi

Publication type:

Article

Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1172, doi. 10.1002/pd.1584

By:

Ezquieta, B.;
Beneyto, M.;
Muñoz-Pacheco, R.;
Barrio, R.;
Oyarzabal, M.;
Lechuga, J. L.;
Luzuriaga, C.;
Hermoso, F.;
Quinteiro, S.;
Martinez, S.

Publication type:

Article

Psychological consequences of prenatal diagnosis in a case of familial Angelman Syndrome.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1156, doi. 10.1002/pd.1577

By:

Turchetti, Daniela;
Razzaboni, Elisabetta;
Zomer, Hila;
Rossi, Cesare;
Ferrari, Simona;
Greco, Donatella;
Graziano, Claudio;
Romeo, Giovanni;
Seri, Marco

Publication type:

Article