Works matching IS 01973851 AND DT 2000 AND VI 20 AND IP 2

Results: 17

Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 132, doi. 10.1002/(SICI)1097-0223(200002)20:2<132::AID-PD765>3.0.CO;2-0

By:

Pigg, Maritta;
Gedde-Dahl, Tobias;
Cox, Diane W.;
Haugen, Guttorm;
Dahl, Niklas

Publication type:

Article

Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case report.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 156, doi. 10.1002/(SICI)1097-0223(200002)20:2<156::AID-PD758>3.0.CO;2-J

By:

Lohmann, L.;
Chelloug, N.;
Rosales, B.;
Guérin, C.;
Lyonnet, S.;
Jonveaux, P.;
Simon-Bouy, B.

Publication type:

Article

Prenatal diagnosis of abdominal enteric duplications.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 163, doi. 10.1002/(SICI)1097-0223(200002)20:2<163::AID-PD769>3.0.CO;2-F

By:

Correia-Pinto, J.;
Tavares, M. L.;
Monteiro, J.;
Moura, N.;
Guimarães, H.;
Estevão-Costa, J.

Publication type:

Article

Relative efficiency of FISH on metaphase and interphase nuclei from non-mosaic trisomic or triploid fibroblast cultures.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 159, doi. 10.1002/(SICI)1097-0223(200002)20:2<159::AID-PD760>3.0.CO;2-2

By:

Ruangvutilert, Pornpimol;
Delhanty, Joy D. A.;
Rodeck, Charles H.;
Harper, Joyce C.

Publication type:

Article

Maternal age-specific rates of Down syndrome used in serum screening are biased low.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 169, doi. 10.1002/(SICI)1097-0223(200002)20:2<169::AID-PD771>3.0.CO;2-W

By:

Hook, Ernest B.

Publication type:

Article

Prenatal diagnosis and management of orofacial clefts.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 149, doi. 10.1002/(SICI)1097-0223(200002)20:2<149::AID-PD764>3.0.CO;2-U

By:

Cockell, Anna;
Lees, Melissa

Publication type:

Article

A false positive diagnosis of conjoined twins in a triplet pregnancy: pitfalls of first trimester ultrasonographic prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 169, doi. 10.1002/(SICI)1097-0223(200002)20:2<169::AID-PD768>3.0.CO;2-C

By:

Usta, Ihab M.;
Awwad, Johnny T.

Publication type:

Article

Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 144, doi. 10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

By:

Hand, Jennifer L.;
Michels, Virginia V.;
Marinello, Michelle J.;
Ketterling, Rhett P.;
Jalal, Syed M.

Publication type:

Article

Current Awareness.

Published in:: Prenatal Diagnosis, 2000, v. 20, n. 2, p. 171, doi. 10.1002/(SICI)1097-0223(200002)20:2<171::AID-PD826>3.0.CO;2-O
Publication type:: Article

Maternal serum second trimester AFP and hCG in pregnancies with placenta previa.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 100, doi. 10.1002/(SICI)1097-0223(200002)20:2<100::AID-PD767>3.0.CO;2-5

By:

Heikkilä, Annaleena;
Heinonen, Seppo;
Kirkinen, Pertti

Publication type:

Article

Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 152, doi. 10.1002/(SICI)1097-0223(200002)20:2<152::AID-PD738>3.0.CO;2-P

By:

Kohlschmidt, Nicolai;
Zielinski, Judith;
Brude, Elke;
Schäfer, Dieter;
Olert, Jürgen;
Hallermann, Christian;
Coerdt, Wiltrud;
Arnemann, Joachim

Publication type:

Article

Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 123, doi. 10.1002/(SICI)1097-0223(200002)20:2<123::AID-PD762>3.0.CO;2-B

By:

Lapierre, Jean-Michel;
Cacheux, Valère;
Luton, Dominique;
Collot, Nathalie;
Oury, Jean-François;
Aurias, Alain;
Tachdjian, Gérard

Publication type:

Article

Plasma measurement of 7-dehydrocholesterol to detect carriers of Smith-Lemli-Opitz syndrome.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 168, doi. 10.1002/(SICI)1097-0223(200002)20:2<168::AID-PD749>3.0.CO;2-C

By:

Nowaczyk, Małgorzata J. M.

Publication type:

Article

Serum screening for Down syndrome and adverse pregnancy outcomes: a case-controlled study.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 96, doi. 10.1002/(SICI)1097-0223(200002)20:2<96::AID-PD766>3.0.CO;2-#

By:

Ogle, Robert;
Jauniaux, Eric;
Pahal, Gurmit S.;
Dell, Elissa;
Sheldrake, Ann;
Rodeck, Charles

Publication type:

Article

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 103, doi. 10.1002/(SICI)1097-0223(200002)20:2<103::AID-PD761>3.0.CO;2-K

By:

Wallerstein, Robert;
Yu, Ming-Tsung;
Neu, Richard L.;
Benn, Peter;
Lee Bowen, Catherine;
Crandall, Barbara;
Disteche, Christine;
Donahue, Roger;
Harrison, Betty;
Hershey, Douglas;
Higgins, Rodney R.;
Jenkins, Lauren S.;
Jackson-Cook, Colleen;
Keitges, Elizabeth;
Khodr, Gabriel;
Lin, C. C.;
Luthardt, Frederick W.;
Meisner, Lorraine;
Mengden, Gregory;
Patil, Shivanand R.

Publication type:

Article

Screening for trisomy 21 in twin pregnancies in the first trimester using free β-hCG and PAPP-A, combined with fetal nuchal translucency thickness.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 91, doi. 10.1002/(SICI)1097-0223(200002)20:2<91::AID-PD759>3.0.CO;2-X

By:

Spencer, Kevin

Publication type:

Article

Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 2, p. 138, doi. 10.1002/(SICI)1097-0223(200002)20:2<138::AID-PD772>3.0.CO;2-2

By:

Li, Marilyn M.;
Howard-Peebles, Patricia N.;
Killos, Lillian D.;
Fallon, Lee;
Listgarten, Eileen;
Stanley, Wayne S.

Publication type:

Article