Works matching IS 01973851 AND DT 2001 AND VI 21 AND IP 10

Results: 24

Semilobar holoprosencephaly in a 46,XY female fetus.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 839, doi. 10.1002/pd.151

By:

Witters, Ingrid;
Moerman, Philippe;
Muenke, Maximilian;
Van Assche, Frans-André;
Devriendt, Koen;
Legius, Eric;
Van Schoubroeck, Dominique;
Fryns, Jean-Pierre

Publication type:

Article

Novel mutations in the human CYP21 gene.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 885, doi. 10.1002/pd.167

By:

Levo, Antti;
Partanen, Jukka

Publication type:

Article

Amnion rupture sequence in a first trimester missed abortion.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 835, doi. 10.1002/pd.150

By:

Philipp, Tom;
Kalousek, Dagmar K.

Publication type:

Article

Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 868, doi. 10.1002/pd.161

By:

Serap Kalkanoğlu, H.;
Romstad, Anne;
Coşkun, Turgay;
Güttler, Flemming

Publication type:

Article

Maternal uniparental heterodisomy for chromosome 2: detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 813, doi. 10.1002/pd.143

By:

Wolstenholme, J.;
White, I.;
Sturgiss, S.;
Carter, J.;
Plant, N.;
Goodship, J. A.

Publication type:

Article

Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 897, doi. 10.1002/pd.154

By:

Hengstschläger, Markus;
Bettelheim, Dieter;
Rosner, Margit;
Repa, Christa;
Deutinger, Josef;
Bernaschek, Gerhard

Publication type:

Article

Successful intrauterine shunting of a sacrococcygeal teratoma (SCT) causing fetal bladder obstruction.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 824, doi. 10.1002/pd.147

By:

Jouannic, Jean-Marie;
Dommergues, Marc;
Auber, Frédéric;
Bessis, Roger;
Nihoul-Fekete, Claire;
Dumez, Yves

Publication type:

Article

Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 860, doi. 10.1002/pd.158

By:

Salafsky, Ira S.;
MacGregor, Scott N.;
Claussen, Uwe;
von Eggeling, Ferdinand

Publication type:

Article

Current Awareness.

Published in:: Prenatal Diagnosis, 2001, v. 21, n. 10, p. 900, doi. 10.1002/pd.15
Publication type:: Article

FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 864, doi. 10.1002/pd.160

By:

Heleen Schuring-Blom, G.;
Hoovers, Jan M. N.;
van Lith, Jan M. M.;
Knegt, Alida C.;
Leschot, Nico J.

Publication type:

Article

Prenatal diagnosis for women aged 37 years and over: to have or not to have.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 842, doi. 10.1002/pd.153

By:

Halliday, Jane L.;
Warren, Rosemary;
McDonald, Geraldine;
Liamputtong Rice, Pranee;
Bell, Robin J.;
Watson, Lyndsey F.

Publication type:

Article

Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 890, doi. 10.1002/pd.175

By:

Morin, Gilles;
Gekas, Jean;
Naepels, Philippe;
Gondry, Jean;
Devauchelle, Bernard;
Testelin, Sylvie;
Sevestre, Henri;
Thépôt, François;
Mathieu, Michèle

Publication type:

Article

Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated α-fetoprotein and cystic renal changes.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 856, doi. 10.1002/pd.157

By:

Chisholm, Christian A.;
Vavelidis, Fotini;
Lovell, Mark A.;
Sweetman, Lawrence;
Roe, Charles R.;
Roe, Diane S.;
Frerman, Frank E.;
Wilson, William G.

Publication type:

Article

Novel feto-specific mRNA species suitable for identification of fetal cells from the maternal circulation.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 806, doi. 10.1002/pd.141

By:

Boye, Kit;
Hougaard, David M.;
Ebbesen, Peter;
Vuust, Jens;
Christiansen, Michael

Publication type:

Article

Prenatal diagnosis in Coffin-Lowry syndrome demonstrates germinal mosaicism confirmed by mutation analysis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 881, doi. 10.1002/pd.163

By:

Horn, Denise;
Delaunoy, Jean-Pierre;
Kunze, Jürgen

Publication type:

Article

A female infant with a 46,XX/48,XY,+8,+10 karyotype in prenatal diagnosis: a 'vanishing twin' phenomenon?

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 896, doi. 10.1002/pd.174

By:

Lloveras, E.;
Lecumberri, J. M.;
Pérez, C.;
Melero, C.;
Zamora, L.;
Sánchez, M. A.;
Solé, F.;
Plaja, A.

Publication type:

Article

Reply to letter.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 895, doi. 10.1002/pd.185

By:

Hackshaw, Allan K.;
Wald, Nicholas J.;
George, Lynne M.

Publication type:

Article

Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 852, doi. 10.1002/pd.156

By:

Tsuchiya, Karen;
Schueler, Mary G.;
Dev, V. G.

Publication type:

Article

Fetal nucleated red blood cells from CVS washings: an aid to development of first trimester non-invasive prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 827, doi. 10.1002/pd.149

By:

Voullaire, Lucille;
Ioannou, Panayiotis;
Nouri, Sara;
Williamson, Robert

Publication type:

Article

Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiency.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 871, doi. 10.1002/pd.162

By:

Niers, L. E. M.;
Smeitink, J. A. M.;
Trijbels, J. M. F.;
Sengers, R. C. A.;
Janssen, A. J. M.;
van den Heuvel, L. P.

Publication type:

Article

Fetal and maternal progenitor cells in co-culture respond equally to erythropoietin.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 818, doi. 10.1002/pd.144

By:

Bohmer, Ralph M.;
Johnson, Kirby L.;
Bianchi, Diana W.

Publication type:

Article

Myomectomy during the first trimester associated with fetal limb anomalies and hydrocephalus in a twin pregnancy.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 848, doi. 10.1002/pd.155

By:

Danzer, E.;
Holzgreve, W.;
Batukan, C.;
Miny, P.;
Tercanli, S.;
Hoesli, I.

Publication type:

Article

Singleton versus duplicate assays in maternal serum screening.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 894, doi. 10.1002/pd.159

By:

Benn, Peter A.

Publication type:

Article

Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 10, p. 801, doi. 10.1002/pd.74

By:

Villa, N.;
Riva, P.;
Colombo, D.;
Sala, E.;
Mariani, S.;
Zorloni, C.;
Crosti, F.;
Dalprà, L.

Publication type:

Article