Works matching IS 01973851 AND DT 2001 AND VI 21 AND IP 8

Results: 23

Prenatal diagnosis of non-obstructive megacystis as part of the megacystis-microcolon-intestinal hypoperistalsis syndrome with favourable postnatal outcome.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 704, doi. 10.1002/pd.114

By:

Witters, Ingrid;
Theyskens, C.;
van Hoestenberghe, Roos;
Sieprath, Peter;
Gyselaers, Wilfried;
Fryns, Jean-Pierre

Publication type:

Article

Current Awareness.

Published in:: Prenatal Diagnosis, 2001, v. 21, n. 8, p. 707, doi. 10.1002/pd.13
Publication type:: Article

Prenatal sonographic appearance of Beare-Stevenson cutis gyrata syndrome: two- and three-dimensional ultrasonographic findings.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 665, doi. 10.1002/pd.136

By:

Hsu, Te-Yao;
Chang, Shiuh-Young;
Wang, Tu-Jou;
Ou, Chia-Yu;
Chen, Zen-Huang;
Hsu, Pei-Hua

Publication type:

Article

The effect of fetal gender on nuchal translucency at 10-14 weeks of gestation.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 627, doi. 10.1002/pd.118

By:

Lam, Yung Hang;
Tang, Mary Hoi Yin;
Lee, Chin Peng;
Sin, Sai Yuen;
Tang, Rebecca;
Wong, Hong Soo;
Wong, Sai Fun

Publication type:

Article

Trisomy 10: ultrasound features and natural history after first trimester diagnosis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 672, doi. 10.1002/pd.129

By:

Brizot, M. L.;
Schultz, R.;
Patroni, L. T.;
Lopes, L. M.;
Armbruster-Moraes, E.;
Zugaib, M.

Publication type:

Article

Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7).

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 642, doi. 10.1002/pd.30

By:

Courtens, W.;
Vroman, S.;
Vandenhove, J.;
Wiedemann, U.;
Schinzel, A.

Publication type:

Article

The effect of fetal gender on second-trimester maternal serum inhibin-A concentration.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 662, doi. 10.1002/pd.120

By:

Hang Lam, Yung;
Hoi Yin Tang, Mary

Publication type:

Article

Expected, prenatally discovered, and born cases of Down syndrome in Denmark during the period 1980-1998.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 630, doi. 10.1002/pd.113

By:

Olesen Larsen, Severin;
Hansen, Jan;
Nørgaard Pedersen, Bent

Publication type:

Article

Reliability of prenatal sonographic lung biometry in the diagnosis of pulmonary hypoplasia.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 649, doi. 10.1002/pd.102

By:

Heling, Kai-Sven;
Tennstedt, Cornelia;
Chaoui, Rabih;
Kalache, Karim D.;
Hartung, John;
Bollmann, Rainer

Publication type:

Article

Changes in fetal heart rate pattern after intrauterine paracentesis in one twin with meconium peritonitis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 693, doi. 10.1002/pd.146

By:

Leung, Wing Cheong;
Pandya, Pranav;
Seaward, Gareth;
Windrim, Rory;
Ryan, Greg

Publication type:

Article

Hepatitis B infection in pregnancy: is it really not harmful to the fetus?

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 701, doi. 10.1002/pd.106

By:

Has, Recep;
Yüksel, Atil;
Topuz, Samet

Publication type:

Article

Fetal cells in the uterine cervix: a source for early non-invasive prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 619, doi. 10.1002/pd.117

By:

Fejgin, Moshe D.;
Diukman, Ron;
Cotton, Yael;
Weinstein, Galina;
Amiel, Aliza

Publication type:

Article

Two- and three-dimensional ultrasound in malformations of the medullary canal: report of four cases.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 622, doi. 10.1002/pd.128

By:

Bonilla-Musoles, Fernando;
Machado, Luis E.;
Osborne, Newton G.;
Muñoz, Elkin A.;
Raga, Francisco;
Blanes, Javier;
Bonilla Jr, Francisco

Publication type:

Article

Second trimester maternal serum analytes in triploid pregnancies: correlation with phenotype and sex chromosome complement.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 680, doi. 10.1002/pd.139

By:

Benn, Peter A.;
Gainey, Andrea;
Ingardia, Charles J.;
Rodis, John F.;
Egan, James F. X.

Publication type:

Article

Prenatal diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 668, doi. 10.1002/pd.112

By:

Regis, Stefano;
Filocamo, Mirella;
Mazzotti, Raffaella;
Cusano, Roberto;
Corsolini, Fabio;
Bonuccelli, Gloria;
Stroppiano, Marina;
Gatti, Rosanna

Publication type:

Article

Carbamoyl phosphate synthetase I deficiency: molecular genetic findings and prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 634, doi. 10.1002/pd.123

By:

Aoshima, Tsutomu;
Kajita, Mitsuharu;
Sekido, Yoshitaka;
Mimura, Shunji;
Itakura, Atsuo;
Yasuda, Izumi;
Saheki, Takeyori;
Watanabe, Kazuyoshi;
Shimokata, Kaoru;
Niwa, Toshimitsu

Publication type:

Article

Heteromorphisms of chromosome 18 can obscure detection of fetal aneuploidy by interphase FISH.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 702, doi. 10.1002/pd.145

By:

Skinner, Jessica L.;
Govberg, Inna J.;
DePalma, Ralph T.;
Cotter, Philip D.

Publication type:

Article

Measurement of inhibin A: a modification to an enzyme-linked immunosorbent assay.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 638, doi. 10.1002/pd.127

By:

Thirunavukarasu, Prema P.;
Wallace, Euan M.

Publication type:

Article

Mild ventriculomegaly in the fetus, natural history, associated findings and outcome of isolated mild ventriculomegaly: a literature review.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 697, doi. 10.1002/pd.138

By:

Kelly, Edmond N.;
Allen, Victoria M.;
Seaward, Gareth;
Windrim, Rory;
Ryan, Greg

Publication type:

Article

Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 676, doi. 10.1002/pd.133

By:

Abrams, Debra J.;
Aronoff, Amy R.;
Ann Berend, Sue;
Roa, Benjamin B.;
Shaffer, Lisa G.;
Geier, Mark R.

Publication type:

Article

Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 613, doi. 10.1002/pd.115

By:

Tabet, A. C.;
Aboura, A.;
Dauge, M. C.;
Audibert, F.;
Coulomb, A.;
Batallan, A.;
Couturier-Turpin, M. H.;
Feldmann, G.;
Tachdjian, G.

Publication type:

Article

The fetal cerebellar vermis: normal development as shown by transvaginal ultrasound.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 687, doi. 10.1002/pd.137

By:

Malinger, G.;
Ginath, S.;
Lerman-Sagie, T.;
Watemberg, N.;
Lev, D.;
Glezerman, M.

Publication type:

Article

Second-trimester maternal serum alpha-fetoprotein (MSAFP) iselevated in women with adverse pregnancy outcome associated with inherited thrombophilias.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 8, p. 658, doi. 10.1002/pd.119

By:

Ochshorn, Yifat;
Kupferminc, Michael J.;
Eldor, Amiram;
Wolman, Igal;
Lessing, Joseph B.;
Yaron, Yuval

Publication type:

Article