Works matching IS 01973851 AND DT 2002 AND VI 22 AND IP 8

Results: 22

Prenatal identification of esophageal atresia: the role of ultrasonography for evaluation of functional anatomy.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 669, doi. 10.1002/pd.375

By:

Shulman, Adrian;
Mazkereth, Rami;
Zalel, Yaron;
Kuint, Jacob;
Lipitz, Shlomo;
Avigad, Itamar;
Achiron, Reuwen

Publication type:

Article

Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 649, doi. 10.1002/pd.370

By:

Silverstein, Shira;
Lerer, Israela;
Sagi, Michal;
Frumkin, Ayala;
Ben-Neriah, Ziva;
Abeliovich, Dvorah

Publication type:

Article

Novel mutation and prenatal sonographic findings of glutaric aciduria (type I) in two Taiwanese families.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 725, doi. 10.1002/pd.392

By:

Lin, S. K.;
Hsu, S. G.;
Ho, E. S. C.;
Tsai, C. R.;
Hseih, Y. T.;
Lo, F. C.;
Lai, H. Y.;
Chen, M. H.

Publication type:

Article

Chondrodysplasia punctata (CDP) with features of the tibia-metacarpal type and maternal phenytoin treatment during pregnancy.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 663, doi. 10.1002/pd.352

By:

Wester, U.;
Brandberg, G.;
Larsson, M.;
Lönnerholm, T.;
Annerén, G.

Publication type:

Article

Outcome of prenatally diagnosed trisomy 6 mosaicism.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 722, doi. 10.1002/pd.391

By:

Wallerstein, Robert;
Oh, Tracey;
Durcan, Judy;
Abdelhak, Yaakov;
Clachko, Mark;
Aviv, Hana

Publication type:

Article

Comparison and integration of first trimester fetal nuchal translucency and second trimester maternal serum screening for fetal Down syndrome.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 730, doi. 10.1002/pd.382

By:

Hang Lam, Yung;
Peng Lee, Chin;
Yuen Sin, Sai;
Tang, Rebecca;
Soo Wong, Hong;
Fun Wong, Sai;
Yee Tak Fong, Danial;
Hoi Yin Tang, Mary;
Hai Nin Woo, Hennie

Publication type:

Article

Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1).

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 652, doi. 10.1002/pd.353

By:

Coulomb L'Herminé, A.;
Aboura, A.;
Simon-Bouy, B.;
Robin, F.;
Audibert, F.;
Strouk, N.;
Capron, F.;
Frydman, R.;
Tachdjian, G.

Publication type:

Article

First trimester screening with free β-hCG, PAPP-A and nuchal translucency in pregnancies conceived with assisted reproduction.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 718, doi. 10.1002/pd.390

By:

Orlandi, Francesco;
Rossi, Cinzia;
Allegra, A.;
Krantz, David;
Hallahan, Terrence;
Orlandi, Emanuela;
Macri, James

Publication type:

Article

Is unexplained third trimester intrauterine death of fetuses with gastroschisis caused by umbilical cord compression due to acute extra-abdominal bowel dilatation?

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 715, doi. 10.1002/pd.386

By:

Kalache, Karim D.;
Bierlich, Anke;
Hammer, Hannes;
Bollmann, Rainer

Publication type:

Article

Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 681, doi. 10.1002/pd.379

By:

Wilson, Susan Clement;
Susman, Marleen;
Bain, Sharon;
Wohlferd, Monica;
Dyke, Daniel L. Van;
Daniel, Art;
White, Beverly;
Gardner, R. J. McKinlay

Publication type:

Article

Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 692, doi. 10.1002/pd.381

By:

Rousseau, Thierry;
Laurent, Nicole;
Thauvin-Robinet, Christel;
Lionnais, Stéphanie;
Durand, Christine;
Faivre, Laurence;
Sagot, Paul

Publication type:

Article

Hypomandibular faciocranial dysostosis in consanguineous parents revealed by ultrasound prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 710, doi. 10.1002/pd.385

By:

Thauvin-Robinet, Christel;
Rousseau, Thierry;
Laurent, Nicole;
Durand, Christine;
Maingueneau, Catherine;
Cormier-Daire, Valérie;
Sagot, Paul;
Faivre, Laurence;
Nivelon-Chevallier, Annie

Publication type:

Article

Current Awareness.

Published in:: Prenatal Diagnosis, 2002, v. 22, n. 8, p. 740, doi. 10.1002/pd.271
Publication type:: Article

Maternal cell contamination in an amniotic fluid sample.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 737, doi. 10.1002/pd.378

By:

McAdoo, Sallie L.;
Bleigh, O. C.;
Simmons, G. Millard;
Wenger, Sharon L.

Publication type:

Article

Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser-induced capillary fluorescence detection.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 686, doi. 10.1002/pd.380

By:

Day, Nancy S.;
Tadin, Marija;
Christiano, Angela M.;
Lanzano, Patricia;
Piomelli, Sergio;
Brown, Stephen

Publication type:

Article

Improved methodology for evaluating nuchal thickness in the second trimester.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 738, doi. 10.1002/pd.389

By:

Cadkin, Alan V.;
Pergament, Eugene

Publication type:

Article

Maternal serum hyperglycosylated human chorionic gonadotrophin (HhCG) in the first trimester of pregnancies affected by Down syndrome, using a sialic acid-specific lectin immunoassay.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 656, doi. 10.1002/pd.351

By:

Spencer, K.;
Talbot, J. A.;
Abushoufa, R. A.

Publication type:

Article

Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 703, doi. 10.1002/pd.384

By:

Savas, S.;
Eraslan, S.;
Kantarci, S.;
Karaman, B.;
Acarsoz, D.;
Tükel, T.;
Cogulu, O.;
Ozkinay, F.;
Basaran, S.;
Aydınlı, K.;
Yuksel-Apak, M.;
Kirdar, B.

Publication type:

Article

Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 736, doi. 10.1002/pd.377

By:

Chen, Chih-Ping;
Chern, Schu-Rern;
Chang, Tung-Yao;
Lin, Chen-Ju;
Wang, Wayseen;
Tzen, Chin-Yuan

Publication type:

Article

Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 697, doi. 10.1002/pd.383

By:

Gilbert, B.;
Yardin, C.;
Briault, S.;
Belin, V.;
Lienhardt, A.;
Aubard, Y.;
Battin, J.;
Servaud, M.;
Philippe, H. J.;
Lacombe, D.

Publication type:

Article

Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 645, doi. 10.1002/pd.354

By:

Graf, Michael D.;
Gill, Prabhcharan;
Krew, Michael;
Schwartz, Stuart

Publication type:

Article

Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.

Published in:

Prenatal Diagnosis, 2002, v. 22, n. 8, p. 675, doi. 10.1002/pd.376

By:

Nataf, V.;
Senat, M. V.;
Albert, M.;
Bidat, L.;
Mazancourt, P. de;
Roume, J.;
Allard, L.;
Tessier, D. Le;
Ville, Y.;
Selva, J.

Publication type:

Article