Works matching IS 01973851 AND DT 2000 AND VI 20 AND IP 10

Results: 22

Prenatal diagnosis of the neuronal ceroid lipofuscinoses.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 819, doi. 10.1002/1097-0223(200010)20:10<819::AID-PD933>3.0.CO;2-M

By:

Kleijer, W. J.;
van Diggelen, O. P.

Publication type:

Article

Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 842, doi. 10.1002/1097-0223(200010)20:10<842::AID-PD915>3.0.CO;2-G

By:

Jakubiczka, Sibylle;
Mitulla, Beate;
Liehr, Thomas;
Arnemann, Joachim;
Lehrach, Hans;
Sudbrak, Ralf;
Stumm, Markus;
Wieacker, Peter F.;
Bettecken, Thomas

Publication type:

Article

Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 847, doi. 10.1002/1097-0223(200010)20:10<847::AID-PD930>3.0.CO;2-O

By:

Zimmermann-Bär, Urs;
Stallmach, Thomas;
Riegel, Mariluce;
Wiedemann, Ute;
Fauchère, Jean-Claude;
Binkert, Franz;
Kotzot, Dieter

Publication type:

Article

First trimester markers of trisomy 21 and the influence of maternal cigarette smoking status.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 852, doi. 10.1002/1097-0223(200010)20:10<852::AID-PD941>3.0.CO;2-M

By:

Spencer, Kevin;
Ong, Charas Y. T.;
Liao, Adolfo W. J.;
Papademetriou, Demetres;
Nicolaides, Kypros H.

Publication type:

Article

Evaluation of the prenatal diagnosis of limb reduction deficiencies.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 811, doi. 10.1002/1097-0223(200010)20:10<811::AID-PD927>3.0.CO;2-J

By:

Stoll, C.;
Wiesel, A.;
Queisser-Luft, A.;
Froster, U.;
Bianca, S.;
Clementi, M.

Publication type:

Article

Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 795, doi. 10.1002/1097-0223(200010)20:10<795::AID-PD897>3.0.CO;2-P

By:

Yan Zhong, Xiao;
Bürk, Martin R.;
Troeger, Carolyn;
Jackson, Laird R.;
Holzgreve, Wolfgang;
Hahn, Sinuhe

Publication type:

Article

High levels of fetal erythroblasts and fetal extracellular DNA in the peripheral blood of a pregnant woman with idiopathic polyhydramnios: case report.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 838, doi. 10.1002/1097-0223(200010)20:10<838::AID-PD911>3.0.CO;2-P

By:

Yan Zhong, Xiao;
Holzgreve, Wolfgang;
Chun Li, Jin;
Aydinli, Kilic;
Hahn, Sinuhe

Publication type:

Article

Response to Hallahan et al.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 790, doi. 10.1002/1097-0223(200010)20:10<790::AID-PD922>3.0.CO;2-C

By:

Haddow, James E.;
Palomaki, Glenn E.;
Knight, George J.

Publication type:

Article

Normal outcome after prenatal diagnosis of thrombosis of the torcular Herophili.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 824, doi. 10.1002/1097-0223(200010)20:10<824::AID-PD926>3.0.CO;2-G

By:

Marc Gicquel, Jean;
Potier, Alain;
Sitruk, Sion;
Girard, Nadine

Publication type:

Article

First trimester biochemical screening for Down syndrome: free beta hCG versus intact hCG.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 785, doi. 10.1002/1097-0223(200010)20:10<785::AID-PD892>3.0.CO;2-6

By:

Hallahan, T.;
Krantz, D.;
Orlandi, F.;
Rossi, C.;
Curcio, P.;
Macri, S.;
Larsen, J.;
Buchanan, P.;
Macri, J.

Publication type:

Article

Combined first trimester nuchal translucency and second trimester biochemical screening tests among normal pregnancies.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 781, doi. 10.1002/1097-0223(200010)20:10<781::AID-PD908>3.0.CO;2-Z

By:

Herman, A.;
Weinraub, Z.;
Dreazen, E.;
Arieli, S.;
Rozansky, S.;
Bukovsky, I.;
Maymon, R.

Publication type:

Article

Current Awareness.

Published in:: Prenatal Diagnosis, 2000, v. 20, n. 10, p. 857, doi. 10.1002/1097-0223(200010)20:10<857::AID-PD834>3.0.CO;2-C
Publication type:: Article

Genetic analysis of fetal nucleated red blood cells from CVS washings.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 832, doi. 10.1002/1097-0223(200010)20:10<832::AID-PD921>3.0.CO;2-U

By:

Jakobs, Marja E.;
van Lith, Jan M. M.;
de Graaf, Irene M.;
Knegt, Alida C.;
Hoovers, Jan M. N.

Publication type:

Article

Fetus with a 9q22q34 interstitial deletion and hygroma.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 855, doi. 10.1002/1097-0223(200010)20:10<855::AID-PD919>3.0.CO;2-Z

By:

Paoloni-Giacobino, A.;
Floris, E.;
Dahoun, S. P.

Publication type:

Article

Sonographic and molecular diagnosis of thanatophoric dysplasia type I at 18 weeks of gestation.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 835, doi. 10.1002/1097-0223(200010)20:10<835::AID-PD903>3.0.CO;2-N

By:

De Biasio, Pierangela;
Prefumo, Federico;
Baffico, Maria;
Baldi, Maurizia;
Priolo, Manuela;
Lerone, Margherita;
Tomà, Paolo;
Luigi Venturini, Pier

Publication type:

Article

False-positive maternal serum screening in systemic lupus erythematosis: a case report.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 851, doi. 10.1002/1097-0223(200010)20:10<851::AID-PD932>3.0.CO;2-L

By:

Ferriman, E. L.;
Sehmi, I. K.;
Jones, R.;
Railton, A.;
Hilton, R. C.;
Cuckle, H. S.

Publication type:

Article

The influence of parity and gravidity on first trimester markers of chromosomal abnormality.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 792, doi. 10.1002/1097-0223(200010)20:10<792::AID-PD914>3.0.CO;2-5

By:

Spencer, K.;
Ong, C. Y. T.;
Liao, A. W. J.;
Nicolaides, K. H.

Publication type:

Article

Management of fetal thyroid goitres: a report of 11 cases in a single perinatal unit.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 799, doi. 10.1002/1097-0223(200010)20:10<799::AID-PD925>3.0.CO;2-V

By:

Volumenie, J. L.;
Polak, M.;
Guibourdenche, J.;
Oury, J. F.;
Vuillard, E.;
Sibony, O.;
Reyal, F.;
Raccah-Tebeka, B.;
Boissinot, C.;
Madec, A. M.;
Orgiazzi, J.;
Toubert, M. E.;
Leger, J.;
Blot, P.;
Luton, D.

Publication type:

Article

Early prenatal diagnosis of the ICF syndrome.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 828, doi. 10.1002/1097-0223(200010)20:10<828::AID-PD907>3.0.CO;2-B

By:

Björck, Erik J.;
Bui, The-Hung;
Wijmenga, Cisca;
Grandell, Ulla;
Nordenskjöld, Magnus

Publication type:

Article

A novel mutation detected by temporal temperature gradient gel electrophoresis led to the confirmative prenatal diagnosis of a Hispanic CF family.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 807, doi. 10.1002/1097-0223(200010)20:10<807::AID-PD929>3.0.CO;2-A

By:

Wong, Lee-Jun C.;
Wang, Jianjun;
Woo, Marilyn;
Hsu, Evelyn;
Michael Bowman, C.

Publication type:

Article

Prenatal diagnosis of X-linked hyper-IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR-mediated site directed mutagenesis.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 822, doi. 10.1002/1097-0223(200010)20:10<822::AID-PD935>3.0.CO;2-K

By:

Jayoussi-Assalia, R.;
Etzioni, A.;
Notarangelo, L.D.;
Brill-Zamir, R.;
Kasinetz, L.;
Kadouri, E;
Gershoni-Baruch, R.

Publication type:

Article

Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 10, p. 854, doi. 10.1002/1097-0223(200010)20:10<854::AID-PD928>3.0.CO;2-1

By:

Wilkin, Helen;
Tuohy, Jeremy;
Theewis, Wilhelmina

Publication type:

Article