Works matching IS 01973851 AND DT 1999 AND VI 19 AND IP 13

Results: 19

Risk of cystic fibrosis with prenatally detected echogenic bowel.

Published in:

1999

By:

Ferriman, E L;
Mason, G;
Ellis, L

Publication type:

Letter

Down syndrome fetal loss rate in early pregnancy.

Published in:

1999

By:

Cuckle, H

Publication type:

Letter

Prenatal diagnosis of bilateral ventriculomegaly and an enlarged cisterna magna in a fetus with partial trisomy 9 and partial trisomy 21.

Published in:

1999

By:

Chen, C P;
Shih, J C

Publication type:

Case Study

First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex.

Published in:

1999

By:

Rouillac, C;
Aral, B;
Fouque, F;
Marchant, D;
Saudubray, J M;
Dumez, Y;
Lindsay, G;
Abitbol, M;
Dufier, J L;
Marsac, C;
Benelli, C

Publication type:

journal article

Fetal scalp cysts--dilemmas in diagnosis.

Published in:

1999

By:

Ogle, R F;
Jauniaux, E

Publication type:

journal article

Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat.

Published in:

1999

By:

Goodman, B K;
Stone, K;
Coddett, J M;
Cargile, C B;
Gurewitsch, E D;
Blakemore, K J;
Stetten, G

Publication type:

journal article

Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCR.

Published in:

1999

By:

Cirigliano, V;
Sherlock, J;
Conway, G;
Quilter, C;
Rodeck, C;
Adinolfi, M

Publication type:

journal article

Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1223, doi. 10.1002/(SICI)1097-0223(199912)19:13<1223::AID-PD724>3.0.CO;2-0

By:

Sermon, K.;
Seneca, S.;
Vanderfaeillie, A.;
Lissens, W.;
Joris, H.;
Vandervorst, M.;
Van Steirteghem, A.;
Liebaers, I.

Publication type:

Article

Invited editorial.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1190, doi. 10.1002/(SICI)1097-0223(199912)19:13<1190::AID-PD735>3.0.CO;2-G

By:

Wells, Dagan

Publication type:

Article

Recent advances and future developments in PGD.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1193, doi. 10.1002/(SICI)1097-0223(199912)19:13<1193::AID-PD728>3.0.CO;2-5

By:

Harper, J. C.;
Wells, D.

Publication type:

Article

Preimplantation genetic diagnosis in 10 couples at risk for transmitting β-thalassaemia major: clinical experience including the initiation of six singleton pregnancies.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1217, doi. 10.1002/(SICI)1097-0223(199912)19:13<1217::AID-PD723>3.0.CO;2-2

By:

Kanavakis, Emmanuel;
Vrettou, Christina;
Palmer, Giles;
Tzetis, Maria;
Mastrominas, Minas;
Traeger-Synodinos, Joanne

Publication type:

Article

Confirmation of diagnosis in preimplantation genetic diagnosis (PGD) through blastocyst culture: preliminary experience.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1242, doi. 10.1002/(SICI)1097-0223(199912)19:13<1242::AID-PD736>3.0.CO;2-P

By:

Veiga, A.;
Gil, Y.;
Boada, M.;
Carrera, M.;
Vidal, F.;
Boiso, I.;
Ménézo, Y.;
Barri, P. N.

Publication type:

Article

Guest editorial.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1189, doi. 10.1002/(SICI)1097-0223(199912)19:13<1189::AID-PD734>3.0.CO;2-D

By:

Harper, J. C.;
Pergament, E.;
Delhanty, J. D. A.

Publication type:

Article

A widely applicable strategy for single cell genotyping of β-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1209, doi. 10.1002/(SICI)1097-0223(199912)19:13<1209::AID-PD722>3.0.CO;2-6

By:

Vrettou, Christina;
Palmer, Giles;
Kanavakis, Emmanuel;
Tzetis, Maria;
Antoniadi, Thalia;
Mastrominas, Minas;
Traeger-Synodinos, Joanne

Publication type:

Article

Successful preimplantation genetic diagnosis for sex linked Lesch-Nyhan syndrome using specific diagnosis.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1237, doi. 10.1002/(SICI)1097-0223(199912)19:13<1237::AID-PD726>3.0.CO;2-O

By:

Ray, Pierre F.;
Harper, Joyce C.;
Ao, Asangla;
Taylor, Deborah M.;
Winston, Robert M. L.;
Hughes, Mark;
Handyside, Alan H.

Publication type:

Article

Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation Δ F508 by fluorescent polymerase chain reaction.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1248, doi. 10.1002/(SICI)1097-0223(199912)19:13<1248::AID-PD737>3.0.CO;2-G

By:

Moutou, Céline;
Viville, Stéphane

Publication type:

Article

Single cell detection of inherited retinoblastoma predisposition.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1231, doi. 10.1002/(SICI)1097-0223(199912)19:13<1231::AID-PD725>3.0.CO;2-X

By:

Sütterlin, Marc;
Sleiman, Patrick Abou;
Onadim, Zerrin;
Delhanty, Joy

Publication type:

Article

An analysis of the demand for and cost of preimplantation genetic diagnosis in the United Kingdom.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1205, doi. 10.1002/(SICI)1097-0223(199912)19:13<1205::AID-PD727>3.0.CO;2-W

By:

Lavery, S. A.;
Aurell, R.;
Turner, C.;
Taylor, D. M.;
Winston, R. M.

Publication type:

Article

The role of the preimplantation geneticist in human cloning.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1200, doi. 10.1002/(SICI)1097-0223(199912)19:13<1200::AID-PD729>3.0.CO;2-V

By:

Fiddler, M.;
Pergament, D.;
Pergament, E.

Publication type:

Article