Works matching IS 01973851 AND DT 2000 AND VI 20 AND IP 13

Results: 18

Urinary hyperglycosylated hCG in first trimester screening for chromosomal abnormalities.

Published in:

2000

By:

Weinans, M J;
Butler, S A;
Mantingh, A;
Cole, L A

Publication type:

journal article

MASA syndrome: ultrasonographic evidence in a male fetus.

Published in:

2000

By:

Pomili, G;
Venti Donti, G;
Alunni Carrozza, L;
Ardisia, C;
Servidio, F;
Hofstra, R M;
Gilardi, G;
Donti, E

Publication type:

journal article

Greenberg dysplasia: first reported case with additional non-skeletal malformations and without consanguinity.

Published in:

2000

By:

Horn, L C;
Faber, R;
Meiner, A;
Piskazeck, U;
Spranger, J

Publication type:

journal article

Prenatal MRI in a fetus with a giant neck hemangioma: a case report.

Published in:

2000

By:

Shiraishi, H;
Nakamura, M;
Ichihashi, K;
Uchida, A;
Izumi, A;
Hyodoh, H;
Momoi, M Y

Publication type:

journal article

Prenatal diagnosis of heterokaryotypic mosaic twins discordant for fetal sex.

Published in:

2000

By:

Schmid, O;
Trautmann, U;
Ashour, H;
Ulmer, R;
Pfeiffer, R A;
Beinder, E

Publication type:

journal article

Quality control in components of comparative genomic hybridization technique used for diagnostic cytogenetic analysis.

Published in:

2000

By:

Loukianova, T A;
Tang, S S;
Kalousek, D K

Publication type:

commentary

Risks of genetic amniocentesis in women less than 35 years old.

Published in:

2000

By:

Ghidini, A;
Prince, M

Publication type:

commentary

High maternal serum inhibin A levels following the loss of one fetus in a twin pregnancy.

Published in:

2000

By:

Goodwin, K M;
Sweeney, P J;
Lambert-Messerlian, G M;
Canick, J A

Publication type:

journal article

Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: ultrasound, molecular cytogenetic and autopsy findings.

Published in:

2000

By:

Froster, U G;
Horn, L C;
Holland, H;
Strenge, S;
Faber, R

Publication type:

journal article

First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1048, doi. 10.1002/1097-0223(200012)20:13<1048::AID-PD975>3.0.CO;2-8

By:

Ray, Pierre F.;
Gigarel, Nadine;
Paul Bonnefont, Jean;
Attié, Tania;
Hamamah, Samir;
Frydman, Nelly;
Vekemans, Michel;
Frydman, René;
Munnich, Arnold

Publication type:

Article

Re-analysis by fluorescence in situ hybridisation of spare embryos cultured until Day 5 after preimplantation genetic diagnosis for a 47, XYY infertile patient demonstrates a high incidence of diploid mosaic embryos: a case report.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1063, doi. 10.1002/1097-0223(200012)20:13<1063::AID-PD982>3.0.CO;2-F

By:

Emiliani, Serena;
Gonzalez Merino, Eric;
Van den Bergh, Marc;
Abramowicz, Marc;
Vassart, Gilbert;
Englert, Yvon;
Delneste, Daniel

Publication type:

Article

Cost-effective screening methods for various single gene defects in single cells using high magnesium and total ionic strength and restriction enzymes.

Published in:

2000

By:

Tsai, Y H

Publication type:

journal article

Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat.

Published in:

2000

By:

Leonard, N J;
Tomkins, D J;
Demianczuk, N

Publication type:

journal article

Use of PRINS for preconception screening of polar bodies for common aneuploidies.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1067, doi. 10.1002/1097-0223(200012)20:13<1067::AID-PD981>3.0.CO;2-E

By:

Petit, Christophe;
Martel-Petit, Véronique;
Fleurentin, Audrey;
Monnier-Barbarino, Patricia;
Jonveaux, Philippe;
Gerard, Hubert

Publication type:

Article

Preimplantation genetic diagnosis of compound heterozygous mutations leading to ablation of plakophilin-1 (PKP1) and resulting in skin fragility ectodermal dysplasia syndrome: a case report.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1055, doi. 10.1002/1097-0223(200012)20:13<1055::AID-PD978>3.0.CO;2-#

By:

Thornhill, Alan R.;
Pickering, Susan J.;
Whittock, Neil V.;
Caller, Jenny;
Andritsos, Vicky;
Bickerstaff, Helen E.;
Handyside, Alan H.;
Eady, Robin A. J.;
Braude, Peter R.;
McGrath, John A.

Publication type:

Article

Guest Editorial.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1029, doi. 10.1002/1097-0223(200012)20:13<1029::AID-PD991>3.0.CO;2-N

By:

Harper, J. C.

Publication type:

Article

Embryo implantation after biopsy of one or two cells from cleavage-stage embryos with a view to preimplantation genetic diagnosis.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1030, doi. 10.1002/1097-0223(200012)20:13<1030::AID-PD977>3.0.CO;2-D

By:

Van de Velde, Hilde;
De Vos, Anick;
Sermon, Karen;
Staessen, Catherine;
De Rycke, Martine;
Van Assche, Elvire;
Lissens, Willy;
Vandervorst, Mark;
Van Ranst, Heidi;
Liebaers, Inge;
Van Steirteghem, André

Publication type:

Article

Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1038, doi. 10.1002/1097-0223(200012)20:13<1038::AID-PD976>3.0.CO;2-8

By:

Iwarsson, Erik;
Malmgren, Helena;
Inzunza, José;
Ährlund-Richter, Lars;
Sjöblom, Peter;
Rosenlund, Björn;
Fridström, Margareta;
Hovatta, Outi;
Nordenskjöld, Magnus;
Blennow, Elisabeth

Publication type:

Article