UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 29

Sortiert nach

A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies

Prenatal diagnosis, 2007-08, Vol.27 (8), p.709-716

2007

Volltextzugriff (PDF)

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?

Prenatal diagnosis, 2015-07, Vol.35 (7), p.663-668

2015

Volltextzugriff (PDF)

Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy

Prenatal diagnosis, 2015-08, Vol.35 (8), p.754-760

2015

Volltextzugriff (PDF)

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)

Prenatal diagnosis, 2005-11, Vol.25 (11), p.1032-1039

2005

Volltextzugriff (PDF)

Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7‐year clinical experience

BJOG : an international journal of obstetrics and gynaecology, 2011-10, Vol.118 (11), p.1340-1348

2011

Volltextzugriff (PDF)

Genomic futures of prenatal screening: ethical reflection

Clinical genetics, 2016-05, Vol.89 (5), p.531-538

2016

Volltextzugriff (PDF)

Noninvasive fetal genotyping of human platelet antigen‐1a

BJOG : an international journal of obstetrics and gynaecology, 2011-10, Vol.118 (11), p.1392-1395

2011

Volltextzugriff (PDF)

Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18

Case reports in genetics, 2015-01, Vol.2015, p.926545-7

2015

Volltextzugriff (PDF)

Detection of Fetal Chromosomal Anomalies: Does Nuchal Translucency Measurement Have Added Value in the Era of Non-invasive Prenatal Testing?

Obstetrical & gynecological survey, 2015-11, Vol.70 (11), p.677-678

2015

Volltextzugriff (PDF)

First-trimester septated cystic hygroma: prevalence, natural history, and pediatric outcome

Obstetrics and gynecology (New York. 1953), 2005-12, Vol.106 (6), p.1415; author reply 1415-1415; author reply 1416

2005

Volltextzugriff (PDF)

Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy: Discordant fetal RHD screening results and vanishing twins

Prenatal diagnosis, 2015-08, Vol.35 (8), p.754-760

2015

Volltextzugriff (PDF)

Receiving the news of Down syndrome in the era of prenatal testing

American journal of medical genetics. Part A, 2020-02, Vol.182 (2), p.374-385

2020

Volltextzugriff (PDF)

The advisory report 'Neonatal screening' from the Health Council of The Netherlands

Nederlands tijdschrift voor geneeskunde, 2005-12, Vol.149 (51), p.2857

2005

Volltextzugriff (PDF)

Sensitivity of fetal RHD screening for safe guidance of targeted anti-D immunoglobulin prophylaxis: prospective cohort study of a nationwide programme in the Netherlands

BMJ (Online), 2016-11, Vol.355, p.i5789

2016

Volltextzugriff (PDF)

Genetic cancer syndromes and reproductive choice: dialogue between parents and politicians on preimplantation genetic diagnosis

Nederlands tijdschrift voor geneeskunde, 2008-07, Vol.152 (27), p.1503

2008

Volltextzugriff (PDF)

Need for blood transfusion in premature infants in 2 Dutch perinatology centres particularly determined by blood sampling for diagnosis

Nederlands tijdschrift voor geneeskunde, 2008-06, Vol.152 (25), p.1419

2008

Volltextzugriff (PDF)

Trends in the utilization of invasive prenatal diagnosis in The Netherlands during 2000-2009

Prenatal diagnosis, 2011-08, Vol.31 (8), p.765-772

2011

Volltextzugriff (PDF)

Factors determining uptake of invasive testing following first-trimester combined testing

Prenatal diagnosis, 2013-04, Vol.33 (4), p.328-333

2013

Volltextzugriff (PDF)

Nieuwe technieken in de obstetrie: detectie van foetaal dna in maternaal bloed

Tijdschrift voor kindergeneeskunde, 2005-08, Vol.73 (4), p.118-122

2005

Volltextzugriff (PDF)

Induction of Labor for Maternal Indications at a Periviable Gestational Age; Survey on Management, Reporting and Auditing amongst Dutch Maternal-Fetal Medicine Specialists and Neonatologists

American journal of perinatology reports, 2018-10, Vol.8 (4), p.e295-e300

2018

Volltextzugriff (PDF)

798: Pregnancy outcome after previous termination of pregnancy for preeclampsia

American journal of obstetrics and gynecology, 2017-01, Vol.216 (1), p.S459-S459

2017

Volltextzugriff (PDF)

Termination of pregnancy for maternal indications at the limits of fetal viability: a retrospective cohort study in the Dutch tertiary care centres

BMJ open, 2014-06, Vol.4 (6), p.e005145-e005145

2014

Volltextzugriff (PDF)

Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy‐14 cotwin

Clinical case reports, 2018-05, Vol.6 (5), p.788-791

2018

Volltextzugriff (PDF)

Cell‐free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case

Clinical case reports, 2015-06, Vol.3 (6), p.489-491

2015

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(23)
Mit Volltextzugriff
(24)

Publikationsform

Artikel
(27)
Berichte
(2)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?

Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)

Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7‐year clinical experience

Genomic futures of prenatal screening: ethical reflection

Noninvasive fetal genotyping of human platelet antigen‐1a

Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18

Detection of Fetal Chromosomal Anomalies: Does Nuchal Translucency Measurement Have Added Value in the Era of Non-invasive Prenatal Testing?

First-trimester septated cystic hygroma: prevalence, natural history, and pediatric outcome

Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy: Discordant fetal RHD screening results and vanishing twins

Receiving the news of Down syndrome in the era of prenatal testing

The advisory report 'Neonatal screening' from the Health Council of The Netherlands

Sensitivity of fetal RHD screening for safe guidance of targeted anti-D immunoglobulin prophylaxis: prospective cohort study of a nationwide programme in the Netherlands

Genetic cancer syndromes and reproductive choice: dialogue between parents and politicians on preimplantation genetic diagnosis

Need for blood transfusion in premature infants in 2 Dutch perinatology centres particularly determined by blood sampling for diagnosis

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study

Trends in the utilization of invasive prenatal diagnosis in The Netherlands during 2000-2009

Factors determining uptake of invasive testing following first-trimester combined testing

Nieuwe technieken in de obstetrie: detectie van foetaal dna in maternaal bloed

Induction of Labor for Maternal Indications at a Periviable Gestational Age; Survey on Management, Reporting and Auditing amongst Dutch Maternal-Fetal Medicine Specialists and Neonatologists

798: Pregnancy outcome after previous termination of pregnancy for preeclampsia

Termination of pregnancy for maternal indications at the limits of fetal viability: a retrospective cohort study in the Dutch tertiary care centres

Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy‐14 cotwin

Cell‐free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case

Suchergebnisse filtern