Works matching IS 01973851 AND DT 2001 AND VI 21 AND IP 1

Results: 19

Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation.

Published in:

2001

By:

Antoniadi, Thalia;
Pampanos, Andreas;
Petersen, Michael B.;
Antoniadi, T;
Pampanos, A;
Petersen, M B

Publication type:

journal article

Fetal hemoglobin-expressing nucleated red blood cell frequencies in pregnancies with intrauterine growth restriction.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 31, doi. 10.1002/1097-0223(200101)21:1<31::AID-PD974>3.0.CO;2-L

By:

Simchen, Michal J.;
Barkai, Gad;
Lusky, Ayala;
Guetta, Esther

Publication type:

Article

Detailed ultrasonographic findings in Greenberg dysplasia.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 65, doi. 10.1002/1097-0223(200101)21:1<65::AID-PD985>3.0.CO;2-4

By:

Madazli, Riza;
Aksoy, Figen;
Ocak, Vildan;
Atasü, Turgay

Publication type:

Article

Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF).

Published in:

2001

By:

Henneman, L.;
Bramsen, I.;
Van Os, Th. A. M.;
Reuling, I. E. W.;
Heyerman, H. G. M.;
van der Laag, J.;
van der Ploeg, H. M.;
ten Kate, L. P.;
Van Os, T A;
Reuling, I E;
Heyerman, H G

Publication type:

journal article

Measuring serum markers once or twice in each assay in antenatal screening for Down syndrome and neural tube defects.

Published in:

2001

By:

Hackshaw, A. K.;
Wald, N. J.;
George, L. M.

Publication type:

Letter

The genetic sonogram: its use in the detection of chromosomal abnormalities in fetuses of women of advanced maternal age.

Published in:

2001

By:

DeVore, Greggory R.;
DeVore, G R

Publication type:

journal article

Current Awareness.

Published in:: Prenatal Diagnosis, 2001, v. 21, n. 1, p. 75, doi. 10.1002/1097-0223(200101)21:1<75::AID-PD6>3.0.CO;2-X
Publication type:: Article

Prenatal diagnosis of disorders of fatty acid transport and mitochondrial oxidation.

Published in:

2001

By:

Rinaldo, P.;
Studinski, A. L.;
Matern, D.

Publication type:

journal article

Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 46, doi. 10.1002/1097-0223(200101)21:1<46::AID-PD984>3.0.CO;2-C

By:

Benn, Peter A.;
Ying, Jun;
Beazoglou, Tryfon;
Egan, James F. X.

Publication type:

Article

Prenatal diagnosis of agnathia-holoprosencephaly: three-dimensional imaging by helical computed tomography.

Published in:

2001

By:

Ebina, Yasuhiko;
Yamada, Hideto;
Hirayama Kato, Emi;
Tanuma, Fumie;
Shimada, Shigeki;
Cho, Kazutoshi;
Fujimoto, Seiichiro;
Ebina, Y;
Yamada, H;
Kato, E H;
Tanuma, F;
Shimada, S;
Cho, K;
Fujimoto, S

Publication type:

journal article

Enrichment and detection of fetal erythroid cells from maternal peripheral blood using liquid culture.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 22, doi. 10.1002/1097-0223(200101)21:1<22::AID-PD987>3.0.CO;2-D

By:

Han, Jin-Yeong;
Lee, Young-Hee;
Sin, Sang-Dong;
Park, Joo-In;
Kim, In-Hoo;
Je, Goo-Hwa;
Rodgers, Griffin P.

Publication type:

Article

Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrum.

Published in:

2001

By:

Witters, Ingrid;
Schreurs, Jan;
Van Wing, Jacques;
Wouters, Werner;
Fryns, Jean-Pierre;
Witters, I;
Schreurs, J;
Van Wing, J;
Wouters, W;
Fryns, J P

Publication type:

journal article

SSCP analysis by RT-PCR for the prenatal diagnosis of Niemann-Pick disease type C.

Published in:

2001

By:

Tsukamoto, Hiroko;
Yamamoto, Toshiyuki;
Nishigaki, Toshinori;
Sakai, Norio;
Nanba, Eiji;
Ninomiya, Haruaki;
Ohno, Kousaku;
Inui, Koji;
Okada, Shintaro;
Tsukamoto, H;
Yamamoto, T;
Nishigaki, T;
Sakai, N;
Nanba, E;
Ninomiya, H;
Ohno, K;
Inui, K;
Okada, S

Publication type:

journal article

Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report.

Published in:

2001

By:

Brown, Lucia Y.;
Alonso, M. Lita;
Yu, Judy;
Warburton, Dorothy;
Brown, Stephen;
Brown, L Y;
Alonso, M L;
Yu, J;
Warburton, D;
Brown, S

Publication type:

journal article

Repeat testing in antenatal screening for Down syndrome using dimeric inhibin-A in combination with other maternal serum markers.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 58, doi. 10.1002/1097-0223(200101)21:1<58::AID-PD964>3.0.CO;2-9

By:

Hackshaw, Allan K.;
Wald, Nicholas J.

Publication type:

Article

Prenatal diagnosis of partial trisomy 3q(3q22-->qter) and monosomy 6q(6q25.3-->qter) in a fetus with sonographic findings of cystic hygromata colli and unilateral pleural effusion.

Published in:

2001

By:

Chen, Chih-Ping;
Chen, C P

Publication type:

Case Study

Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy.

Published in:

2001

By:

Kuchinka, B. D.;
Barrett, I. J.;
Moya, G.;
Sánchez, J. M.;
Langlois, S.;
Yong, S.-L.;
Kalousek, D. K.;
Robinson, W. P.;
Sánchez, J M

Publication type:

journal article

A. Farina, N. Rizzo, G. Simonazzi, P. Calderoni, P. Carinci and L. Bovicelli, 'Survival analysis of transfused fetuses affected by Rh-alloimmunization'. Prenatal Diagnosis 20(11) 2000, 881-885.

Published in:: Prenatal Diagnosis, 2001, v. 21, n. 1, p. 74, doi. 10.1002/1097-0223(200101)21:1<74::AID-PD40>3.0.CO;2-U
Publication type:: Article

Relationship between gestational age and frequency of fetal trophoblasts and nucleated erythrocytes in maternal peripheral blood.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 14, doi. 10.1002/1097-0223(200101)21:1<14::AID-PD970>3.0.CO;2-#

By:

Hui Lim, Tse;
Sian Ann Tan, Ann;
Hng Hang Goh, Victor

Publication type:

Article