Works matching IS 01973851 AND DT 2002 AND VI 22 AND IP 6

Results: 21

Mucopolysaccharidosis VII (Sly disease) as a cause of increased nuchal translucency and non-immune fetal hydrops: study of a family and technical approach to prenatal diagnosis in early and late pregnancy.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 493, doi. 10.1002/pd.330

By:

Geipel, A.;
Berg, C.;
Germer, U.;
Krapp, M.;
Kohl, M.;
Gembruch, U.

Publication type:

Article

In utero first trimester exposure to low-dose methotrexate with increased fetal nuchal translucency and associated malformations.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 489, doi. 10.1002/pd.334

By:

Krähenmann, F.;
Østensen, M.;
Stallmach, Th.;
Huch, A.;
Chaoui, R.

Publication type:

Article

Trisomy 18 in a fetus with normal NT and abnormal maternal serum biochemistry.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 492, doi. 10.1002/pd.338

By:

De Biasio, Pierangela;
Canini, Silvana;
Prefumo, Federico;
Luigi Venturini, Pier

Publication type:

Article

Application of monopolar thermocoagulation in an acardiac fetus.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 499, doi. 10.1002/pd.349

By:

Chao, An-Shine;
Hsieh, Ching-Chang;
Liou, Jui-Der;
Soong, Yung-Kuei

Publication type:

Article

Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluid.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 456, doi. 10.1002/pd.344

By:

Chadefaux-Vekemans, B.;
Rabier, D.;
Chabli, A.;
Blanc, A.;
Aupetit, J.;
Bardet, J.;
Kamoun, P.

Publication type:

Article

Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 512, doi. 10.1002/pd.388

By:

Wilton, Leeanda;
Harper, Joyce

Publication type:

Article

Non-disclosing preimplantation genetic diagnosis for Huntington disease.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 503, doi. 10.1002/pd.359

By:

Stern, Harvey J.;
Harton, Gary L.;
Sisson, Michael E.;
Jones, Shirley L.;
Fallon, Lee A.;
Thorsell, Lilli P.;
Getlinger, Michael E.;
Black, Susan H.;
Schulman, Joseph D.;
Harper, Joyce

Publication type:

Article

Expandability of haemopoietic progenitors in first trimester fetal and maternal blood: implications for non-invasive prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 463, doi. 10.1002/pd.350

By:

Campagnoli, Cesare;
Roberts, Irene A. G.;
Kumar, Sailesh;
Choolani, Mahesh;
Bennett, Phillip R.;
Letsky, Elizabeth;
Fisk, Nicholas M.

Publication type:

Article

Brain anomalies associated with 47,XYY karyotypes detected on a prenatal scan.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 490, doi. 10.1002/pd.332

By:

Maymon, R.;
Herman, A.;
Reish, O.

Publication type:

Article

First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13).

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 487, doi. 10.1002/pd.343

By:

Martin-Denavit, T.;
Attia-Sobol, J.;
Theuil, J.;
Abel-Lablanche, K.;
Boggio, D.;
Teyssier, M.;
Till, M.;
Champion, F.;
Vitrey, D.;
Plauchu, H.

Publication type:

Article

Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 525, doi. 10.1002/pd.394

By:

Harper, Joyce C.;
Wells, Dagan;
Piyamongkol, Wirawit;
Abou-Sleiman, Patrick;
Apessos, Angela;
Ioulianos, Antonis;
Davis, Mary;
Doshi, Alpesh;
Serhal, Paul;
Ranieri, Massimo;
Rodeck, Charles;
Delhanty, Joy D. A.;
Harper, Joyce

Publication type:

Article

An increase in cost-effectiveness of first trimester maternal screening programmes for fetal chromosome anomalies is obtained by contingent testing.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 482, doi. 10.1002/pd.336

By:

Christiansen, Michael;
Olesen Larsen, Severin

Publication type:

Article

Attitude of at-risk subjects towards preimplantation genetic diagnosis of α- and β-thalassaemias in Hong Kong.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 508, doi. 10.1002/pd.387

By:

Wah Hui, Pui;
Lam, Yung Hang;
Chen, Min;
Tang, Mary Hoi Yin;
Yeung, William Shu Biu;
Ng, Ernest Hung Yu;
Ho, Pak Chung;
Harper, Joyce

Publication type:

Article

The role of hyperglycosylated hCG in trophoblast invasion and the prediction of subsequent pre-eclampsia.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 478, doi. 10.1002/pd.329

By:

Bahado-Singh, R. O.;
Oz, A. U.;
Kingston, J. M.;
Shahabi, S.;
Hsu, C. D.;
Cole, L.

Publication type:

Article

Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 497, doi. 10.1002/pd.299

By:

Liehr, Thomas;
Schreyer, Isolde;
Neumann, Annett;
Beensen, Volkmar;
Ziegler, Monika;
Hartmann, Isabell;
Starke, Heike;
Heller, Anita;
Nietzel, Angela;
Claussen, Uwe

Publication type:

Article

Pallister-Killian syndrome: difficulties of prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 470, doi. 10.1002/pd.342

By:

Doray, Bérénice;
Girard-Lemaire, Françoise;
Gasser, Bernard;
Baldauf, Jean-Jacques;
de Geeter, Bernard;
Spizzo, Michèle;
Zeidan, Charles;
Flori, Elisabeth

Publication type:

Article

First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2).

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 519, doi. 10.1002/pd.393

By:

Abou-Sleiman, P. M.;
Apessos, A.;
Harper, J. C.;
Serhal, P.;
Winston, R. M. L.;
Delhanty, J. D. A.;
Harper, Joyce

Publication type:

Article

Pilot study for the neonatal screening of fragile X syndrome.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 459, doi. 10.1002/pd.346

By:

Rifé, M.;
Mallolas, J.;
Badenas, C.;
Tazón, B.;
Miguélez, M. Rodríguez;
Pàmpols, T.;
Sànchez, A.;
Milà, M.

Publication type:

Article

Varix of the portal vein: prenatal diagnosis in a fetus with mosaic trisomy 9 syndrome.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 495, doi. 10.1002/pd.317

By:

Tseng, Jenn-Jhy;
Chou, Min-Min;
Shih-Chu Ho, Esther

Publication type:

Article

Invasive testing for the karyotyping of mid-trimester intrauterine fetal death (IUFD): a pilot study.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 6, p. 453, doi. 10.1002/pd.339

By:

Howarth, E. S.;
Konje, J. C.;
Healey, K. A.;
Duckett, D. P.;
Scudamore, I. W.;
Taylor, D. J.

Publication type:

Article

Current Awareness.

Published in:: Prenatal Diagnosis, 2002, v. 22, n. 6, p. 534, doi. 10.1002/pd.269
Publication type:: Article