Works matching IS 01973851 AND DT 2000 AND VI 20 AND IP 11

Results: 20

Cytogenetic discrepancy between fetal tissue and body fluid in a fetus with cystic hygroma colli.

Published in:

2000

By:

Chen, Chih-Ping;
Chen, C P

Publication type:

Case Study

Survival analysis of transfused fetuses affected by Rh-alloimmunization.

Published in:

2000

By:

Farina, Antonio;
Calderoni, Patrizio;
Simonazzi, Giuliana;
Carinci, Paolo;
Rizzo, Nicola;
Farina, A;
Calderoni, P;
Simonazzi, G;
Carinci, P;
Rizzo, N

Publication type:

journal article

Isolated polydactyly: prenatal diagnosis and perinatal outcome.

Published in:

2000

By:

Bromley, Bryann;
Shipp, Thomas D.;
Benacerraf, Beryl;
Bromley, B;
Shipp, T D;
Benacerraf, B

Publication type:

journal article

The subarachnoid space: normal fetal development as demonstrated by transvaginal ultrasound.

Published in:

2000

By:

Malinger, Gustavo;
Lerman-Sagie, Tally;
Achiron, Reuwen;
Lipitz, Shlomo;
Malinger, G;
Lerman-Sagie, T;
Achiron, R;
Lipitz, S

Publication type:

journal article

Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegaly.

Published in:

2000

By:

Robinet, Christel;
Douvier, Serge;
Khau Van Kien, Philippe;
Favre, Bernardine;
Luquet, Isabelle;
Nadal, Nathalie;
Nivelon-Chevallier, Annie;
Mugneret, Francine;
Robinet, C;
Douvier, S;
Khau Van Kien, P;
Favre, B;
Luquet, I;
Nadal, N;
Nivelon-Chevallier, A;
Mugneret, F

Publication type:

Case Study

Current Awareness.

Published in:: Prenatal Diagnosis, 2000, v. 20, n. 11, p. 939, doi. 10.1002/1097-0223(200011)20:11<939::AID-PD835>3.0.CO;2-A
Publication type:: Article

Axial growth of the fetal eye and evaluation of the hyaloid artery: in utero ultrasonographic study.

Published in:

2000

By:

Achiron, Reuwen;
Kreiser, Doron;
Achiron, Anat;
Achiron, R;
Kreiser, D;
Achiron, A

Publication type:

journal article

Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 11, p. 870, doi. 10.1002/1097-0223(200011)20:11<870::AID-PD940>3.0.CO;2-J

By:

Clementi, Maurizio;
Tenconi, Romano;
Bianchi, Fabrizio;
Stoll, Claude

Publication type:

Article

Prenatal diagnosis of haemoglobin Bart's disease by cordocentesis at 12-14 weeks-experience with the first 59 cases.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 11, p. 900, doi. 10.1002/1097-0223(200011)20:11<900::AID-PD944>3.0.CO;2-R

By:

Hang Lam, Yung;
Hoi Yin Tang, Mary

Publication type:

Article

A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomy.

Published in:

2000

By:

Slater, Howard R.;
Ralph, Adrianne;
Daniel, Art;
Worthington, Sharron;
Roberts, Cynthia;
Slater, H R;
Ralph, A;
Daniel, A;
Worthington, S;
Roberts, C

Publication type:

journal article

An unusual case of trisomy and triploidy in a chorion villus biopsy.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 11, p. 917, doi. 10.1002/1097-0223(200011)20:11<917::AID-PD937>3.0.CO;2-9

By:

English, C. J.;
Atkey, N. W. S.;
Linton, G.;
Napier, C. J.;
Cameron, H. M.;
Mason, G. C.;
Murray, B. J.

Publication type:

Article

Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis.

Published in:

2000

By:

Mandel, H.;
Abeling, N.;
Gutman, A.;
Berant, M.;
Scholten, E. G.;
Sheiman, C.;
Luder, A.;
van Gennip, A. H.

Publication type:

journal article

Prenatal diagnosis of a novel COL1A1 mutation in osteogenesis imperfecta type I carried through full term pregnancy.

Published in:

2000

By:

Ries, Liat;
Frydman, Moshe;
Barkai, Gad;
Goldman, Boleslaw;
Friedman, Eitan;
Ries, L;
Frydman, M;
Barkai, G;
Goldman, B;
Friedman, E

Publication type:

journal article

3-M syndrome: a prenatal ultrasonographic diagnosis.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 11, p. 921, doi. 10.1002/1097-0223(200011)20:11<921::AID-PD947>3.0.CO;2-B

By:

Meo, Francesco;
Pinto, Vincenzo;
D'Addario, Vincenzo

Publication type:

Article

Hyperechogenic bowel in the second trimester fetus: a review.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 11, p. 909, doi. 10.1002/1097-0223(200011)20:11<909::AID-PD918>3.0.CO;2-9

By:

Penna, Leonie;
Bower, Sarah

Publication type:

Article

Prenatally detected true double trisomy mosaic 12 and 13 not confirmed in fetal and placental tissues by conventional cytogenetic methods, but suggested by FISH analysis.

Published in:

2000

By:

Djalali, M.;
Merk, O.;
Storli, K.;
Vogel, W.

Publication type:

Case Study

The practical importance of pedigree analysis in women considering invasive prenatal diagnosis for advanced maternal age or abnormal serum screening tests.

Published in:

2000

By:

Meschede, D.;
Albersmann, S.;
Horst, J.

Publication type:

journal article

Apoptosis in fetal nucleated erythrocytes circulating in maternal blood.

Published in:

2000

By:

Sekizawa, Akihiko;
Samura, Osamu;
Zhen, DongKai;
Falco, Vincent;
Farina, Antonio;
Bianchi, Diana W.;
Sekizawa, A;
Samura, O;
Zhen, D K;
Falco, V;
Farina, A;
Bianchi, D W

Publication type:

journal article

Transposition of the great arteries, ventricular septal defect and diaphragmatic hernia in a fetus: the role of prenatal diagnosis in helping to predict postnatal survival.

Published in:

2000

By:

Noimark, Lee;
Sellwood, Mark;
Wyatt, John;
Yates, Robert;
Noimark, L;
Sellwood, M;
Wyatt, J;
Yates, R

Publication type:

journal article

Retrospective diagnosis of trisomy 15 in formalin-fixed, paraffin-embedded placental tissue in a newborn girl with Prader-Willi syndrome.

Published in:

2000

By:

Walczak, Claudia;
Enders, Herbert;
Grissinger, Klaus;
Dufke, Andreas;
Walczak, C;
Enders, H;
Grissinger, K;
Dufke, A

Publication type:

journal article