Works matching IS 01973851 AND DT 2004 AND VI 24 AND IP 8

Results: 20

Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 647, doi. 10.1002/pd.962

By:

Sensi, A.;
Cavani, S.;
Villa, N.;
Pomponi, M. G.;
Fogli, A.;
Gualandi, F.;
Grasso, M.;
Sala, E.;
Pietrobono, R.;
Baldinotti, F.;
Savin, E.;
Ferlini, A.;
Cecconi, M.;
Rossi, S.;
Gallone, S.;
Bellini, C.;
Neri, G.;
Martinoli, E.;
Simi, P.;
Dalprà, L.

Publication type:

Article

Prenatal diagnosis of Lesch-Nyhan disease.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 658, doi. 10.1002/pd.885

By:

Kleijer, W. J.;
van den Berg, P.;
Los, F. J.

Publication type:

Article

First-trimester diagnosis of hydrolethalus syndrome in a Chinese family.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 587, doi. 10.1002/pd.870

By:

Chan, Ben Chong Pun;
Shek, Tony Wai Hung;
Lee, Chin Peng

Publication type:

Article

A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidum.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 635, doi. 10.1002/pd.955

By:

Delcán, José;
Orera, María;
Linares, Rafael;
Saavedra, Dolores;
Palomar, Angustias

Publication type:

Article

Congenital malformations of the diaphragm: findings of the West Midlands Congenital Anomaly Register 1995 to 2000.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 596, doi. 10.1002/pd.908

By:

Tonks, A.;
Wyldes, M.;
Somerset, D. A.;
Dent, K.;
Abhyankar, A.;
Bagchi, I.;
Lander, A.;
Roberts, E.;
Kilby, M. D.

Publication type:

Article

The impact of fetal renal pelvic diameter on postnatal outcome.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 591, doi. 10.1002/pd.899

By:

John, Ulrike;
Kähler, Christiane;
Schulz, Sven;
Mentzel, Hans Joachim;
Vogt, Susanna;
Misselwitz, Joachim

Publication type:

Article

Prenatal diagnosis of tetrasomy 9p with Dandy-Walker malformation.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 623, doi. 10.1002/pd.933

By:

Hengstschläger, Markus;
Bettelheim, Dieter;
Drahonsky, Regina;
Repa, Christa;
Deutinger, Josef;
Bernaschek, Gerhard

Publication type:

Article

The relationship between maternal serum alpha-fetoprotein and maternal haemoglobin.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 609, doi. 10.1002/pd.921

By:

Bartha, Jose L.;
Omar, Kiria M.;
Soothill, Peter W.

Publication type:

Article

First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 631, doi. 10.1002/pd.954

By:

Coviello, Domenico A.;
Brambati, Bruno;
Tului, Lucia;
Percesepe, Antonio;
Sironi, Francesca;
Sahai, Achal;
Bertorelli, Roberto;
Forabosco, Antonino

Publication type:

Article

Prenatal exclusion without involving the putative fathers of an incestuous father-daughter parenthood.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 662, doi. 10.1002/pd.929

By:

Schmidtke, J.;
Kühnau, W.;
Wand, D.;
Edelmann, J.;
Szibor, R.;
Krawczak, M.

Publication type:

Article

Sonography in prenatal diagnosis of congenital adrenal hyperplasia.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 627, doi. 10.1002/pd.948

By:

Saada, Julien;
Grebille, Anne-Gaëlle;
Aubry, Marie-Cécile;
Rafii, Arash;
Dumez, Yves;
Benachi, Alexandra

Publication type:

Article

Safety of fetal blood sampling by cordocentesis in fetuses with single umbilical arteries.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 605, doi. 10.1002/pd.920

By:

Abdel-Fattah, Sherif A.;
Bartha, Jose L.;
Kyle, Phillipa M.;
Denbow, Mark L.;
Soothill, Peter W.

Publication type:

Article

Prenatal diagnosis of Pfeiffer syndrome type II.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 644, doi. 10.1002/pd.960

By:

Blaumeiser, Bettina;
Loquet, Philip;
Wuyts, Wim;
Nöthen, Markus M.

Publication type:

Article

Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 619, doi. 10.1002/pd.931

By:

Di Giacomo, Marilena C.;
Cesarano, Carla;
Bukvic, Nenad;
Manisali, Evangelia;
Guanti, Ginevra;
Susca, Francesco

Publication type:

Article

Prenatal diagnosis of mosaic 22q11.2 microdeletion.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 660, doi. 10.1002/pd.917

By:

Chen, Chih-Ping;
Chern, Schu-Rern;
Lee, Chen-Chi;
Lin, Shuan-Pei;
Chang, Tung-Yao;
Wang, Wayseen

Publication type:

Article

Increased rate of aneuploid embryos in young women with previous aneuploid conceptions.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 638, doi. 10.1002/pd.957

By:

Munné, Santiago;
Sandalinas, Mireia;
Magli, Cristina;
Gianaroli, Luca;
Cohen, Jacques;
Warburton, Dorothy

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2004, v. 24, n. 8, p. 665, doi. 10.1002/pd.780
Publication type:: Article

Randomised trial comparing an interactive multimedia decision aid with a leaflet and a video to give information about prenatal screening for Down syndrome.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 613, doi. 10.1002/pd.927

By:

Leung, K. Y.;
Lee, C. P.;
Chan, H. Y.;
Tang, M. H. Y.;
Lam, Y. H.;
Lee, A.

Publication type:

Article

Investigation of lysosomal storage diseases in nonimmune hydrops fetalis.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 653, doi. 10.1002/pd.967

By:

Burin, Maira G.;
Scholz, Ana P.;
Gus, Rejane;
Sanseverino, Maria Teresa V.;
Fritsh, Alessandra;
Magalhães, José A.;
Timm, Fernanda;
Barrios, Patrícia;
Chesky, Marisa;
Coelho, Janice C.;
Giugliani, Roberto

Publication type:

Article

Reply: Prenatal diagnosis of Lesch-Nyhan disease.

Published in:

Prenatal Diagnosis, 2004, v. 24, n. 8, p. 659, doi. 10.1002/pd.886

By:

Nyhan, William L.

Publication type:

Article