Works matching IS 01973851 AND DT 1999 AND VI 19 AND IP 6

Results: 21

Appropriate biochemical parameters in first-trimester screening for Down syndrome.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 505, doi. 10.1002/(SICI)1097-0223(199906)19:6<505::AID-PD572>3.0.CO;2-6

By:

Cuckle, Howard S.;
van Lith, Jan M. M.

Publication type:

Article

Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisis.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 580, doi. 10.1002/(SICI)1097-0223(199906)19:6<580::AID-PD583>3.0.CO;2-K

By:

Donaldson, Susan J. F.;
Wright, Colleen A.;
de Ravel, Thomy J. L.

Publication type:

Article

High failure rate of umbilical vessel occlusion by ultrasound-guided injection of absolute alcohol or enbucrilate gel.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 527, doi. 10.1002/(SICI)1097-0223(199906)19:6<527::AID-PD576>3.0.CO;2-N

By:

Denbow, M. L.;
Overton, T. G.;
Duncan, K. R.;
Cox, P. M.;
Fisk, N. M.

Publication type:

Article

First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysis.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 559, doi. 10.1002/(SICI)1097-0223(199906)19:6<559::AID-PD587>3.0.CO;2-8

By:

de Vries, B. B. A.;
Kleijer, W. J.;
Keulemans, J. L. M.;
Voznyi, Y. V.;
Franken, P. F.;
Eurlings, M. C. M.;
Galjaard, R. J.;
Losekoot, M.;
Catsman-Berrevoets, C. E.;
Breuning, M. H.;
Taschner, P. E. M.;
van Diggelen, O. P.

Publication type:

Article

Fetal cardiac abnormalities and their association with aneuploidy.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 563, doi. 10.1002/(SICI)1097-0223(199906)19:6<563::AID-PD605>3.0.CO;2-M

By:

Yates, R.

Publication type:

Article

A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 570, doi. 10.1002/(SICI)1097-0223(199906)19:6<570::AID-PD582>3.0.CO;2-Q

By:

Brackley, K. J.;
Kilby, M. D.;
Morton, J.;
Whittle, M. J.;
Knight, S. J. L.;
Flint, J.

Publication type:

Article

Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 542, doi. 10.1002/(SICI)1097-0223(199906)19:6<542::AID-PD586>3.0.CO;2-L

By:

Chessa, L.;
Piane, M.;
Prudente, S.;
Carducci, C.;
Mazzilli, M. C.;
Pachtì, A.;
Negrini, M.;
Narducci, M. G.;
Russo, G.;
Frati, L.

Publication type:

Article

Maternal serum activin A and follistatin levels in pregnancies with Down syndrome.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 513, doi. 10.1002/(SICI)1097-0223(199906)19:6<513::AID-PD579>3.0.CO;2-L

By:

Cuckle, H. S.;
Sehmi, I.;
Jones, R.;
Evans, L. W.

Publication type:

Article

Haemolytic disease of the newborn caused by anti-c, anti-E and anti-Fya antibodies: report of five cases.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 533, doi. 10.1002/(SICI)1097-0223(199906)19:6<533::AID-PD570>3.0.CO;2-5

By:

Babinszki, Agota;
Berkowitz, Richard L.

Publication type:

Article

The prenatal diagnosis of Pierre-Robin sequence.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 567, doi. 10.1002/(SICI)1097-0223(199906)19:6<567::AID-PD581>3.0.CO;2-P

By:

Hsieh, Yao-Yuan;
Chang, Chi-Chen;
Tsai, Horng-Der;
Yang, Tung-Chuan;
Lee, Chien-Chung;
Tsai, Chang-Hai

Publication type:

Article

Prenatal detection of a giant bilateral thoracic vascular lesion: prognostic evaluation and genetic aspects.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 583, doi. 10.1002/(SICI)1097-0223(199906)19:6<583::AID-PD585>3.0.CO;2-B

By:

Meiner, A.;
Faber, R.;
Horn, L.-C.;
Reichenbach, H.;
Froster, U. G.

Publication type:

Article

Evolution of the centromeric alpha-satellite DNA sequences of human chromosome 22.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 590, doi. 10.1002/(SICI)1097-0223(199906)19:6<590::AID-PD567>3.0.CO;2-7

By:

Verma, Ram S.

Publication type:

Article

A comparison of different density gradients and antibodies for enrichment of fetal erythroblasts by MACS.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 521, doi. 10.1002/(SICI)1097-0223(199906)19:6<521::AID-PD578>3.0.CO;2-N

By:

Troeger, Carolyn;
Holzgreve, Wolfgang;
Hahn, Sinuhe

Publication type:

Article

Maternal serum screening for Down syndrome in the first trimester: experience from Belarus.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 499, doi. 10.1002/(SICI)1097-0223(199906)19:6<499::AID-PD555>3.0.CO;2-6

By:

Tsukerman, G. L.;
Gusina, N. B.;
Cuckle, H. S.

Publication type:

Article

Prenatal diagnosis of tuberous sclerosis with intracerebral signs at 14 weeks' gestation.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 575, doi. 10.1002/(SICI)1097-0223(199906)19:6<575::AID-PD580>3.0.CO;2-R

By:

Brackley, K. J.;
Farndon, P. A.;
Weaver, J. B.;
Dow, D. J.;
Chapman, S.;
Kilby, M. D.

Publication type:

Article

SP1 in pregnancies with Down syndrome in the first trimester of pregnancy.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 517, doi. 10.1002/(SICI)1097-0223(199906)19:6<517::AID-PD591>3.0.CO;2-2

By:

Wald, N. J.;
Watt, H. C.;
Norgaard-Pedersen, B.;
Christiansen, M.

Publication type:

Article

Maternal serum pregnancy-associated plasma protein A (PAPP-A) but not pregnancy-specific β1-glycoprotein (SP1) is a useful second-trimester marker for fetal trisomy 18.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 537, doi. 10.1002/(SICI)1097-0223(199906)19:6<537::AID-PD573>3.0.CO;2-T

By:

Bersinger, N. A.;
Leporrier, N.;
Herrou, M.;
Leymarie, P.

Publication type:

Article

The association of increased fetal nuchal translucency and spinal muscular atrophy type I.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 587, doi. 10.1002/(SICI)1097-0223(199906)19:6<587::AID-PD584>3.0.CO;2-A

By:

Stiller, Robert J.;
Lieberson, Dara;
Herzlinger, Robert;
Siddiqui, Danish;
Laifer, Steven A.;
Whetham, John C. G.

Publication type:

Article

Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 546, doi. 10.1002/(SICI)1097-0223(199906)19:6<546::AID-PD589>3.0.CO;2-8

By:

Morris, A.;
Boyd, E.;
Dhanjal, S.;
Lowther, G. W.;
Aitken, D. A.;
Young, J.;
Menzies, A. L.;
Imrie, S. J.;
Connor, J. M.

Publication type:

Article

Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 591, doi. 10.1002/(SICI)1097-0223(199906)19:6<591::AID-PD577>3.0.CO;2-5

By:

Chen, Chih-Ping

Publication type:

Article

Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 6, p. 552, doi. 10.1002/(SICI)1097-0223(199906)19:6<552::AID-PD588>3.0.CO;2-C

By:

Houštěk, Josef;
Klement, Petr;
Heřmanská, Jana;
Antonická, Hana;
Houšťková, Hana;
Stratilová, Leona;
Wanders, Ronald J. A.;
Zeman, Jiří

Publication type:

Article