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Long-term psychological consequences of pregnancy termination for fetal abnormality: a cross-sectional study

Prenatal diagnosis, 2005-03, Vol.25 (3), p.253-260

2005

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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

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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

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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

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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

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Detection of fetal RHD-specific sequences in maternal plasma

The Lancet (British edition), 1998-10, Vol.352 (9135), p.1196-1196

1998

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Earliest gestational age for fetal sexing in cell-free maternal plasma

Prenatal diagnosis, 2003-12, Vol.23 (13), p.1042-1044

2003

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Does 17‐α‐hydroxyprogesterone caproate affect fetal biometry and birth weight in twin pregnancy?

Ultrasound in obstetrics & gynecology, 2013-09, Vol.42 (3), p.329-334

2013

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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

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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

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Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12)

Prenatal diagnosis, 2003-01, Vol.23 (1), p.65-67

2003

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Adverse obstetric outcome in low- and high-risk pregnancies: predictive value of maternal serum screening

Obstetrics and gynecology (New York. 1953), 1999-12, Vol.94 (6), p.929-934

1999

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Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

Prenatal diagnosis, 2003-09, Vol.23 (9), p.747-751

2003

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Antiepileptic drug regimens and major congenital abnormalities in the offspring

Annals of neurology, 1999-11, Vol.46 (5), p.739-746

1999

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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

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Comparative genomic hybridization for cytogenetic evaluation of stillbirth

Obstetrics and gynecology (New York. 1953), 2000-08, Vol.96 (2), p.281-286

2000

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)

Does 17-[alpha]-hydroxyprogesterone caproate affect fetal biometry and birth weight in twin pregnancy?

Ultrasound in obstetrics & gynecology, 2013-09, Vol.42 (3), p.329-334

2013

Volltextzugriff (PDF)

Long-term Psychological Consequences of Pregnancy Termination for Fetal Abnormality: A Cross-sectional Study

Obstetrical & gynecological survey, 2005-09, Vol.60 (9), p.568-570

2005

Volltextzugriff (PDF)

SUCCESSFUL TREATMENT OF ACUTE PROMYELOCYTIC LEUKAEMIA WITH ALL‐TRANS‐RETINOIC‐ACID DURING LATE PREGNANCY

British journal of haematology, 1996-09, Vol.94 (4), p.699-701

1996

Volltextzugriff (PDF)

MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME 22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY 22

Prenatal diagnosis, 1997-01, Vol.17 (1), p.81-86

1997

Volltextzugriff (PDF)

Comparison of platelet counts in first and second newborns of mothers with immune thrombocytopenic purpura

Obstetrics and gynecology (New York. 1953), 1997-10, Vol.90 (4), p.546-552

1997

Volltextzugriff (PDF)

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Long-term psychological consequences of pregnancy termination for fetal abnormality: a cross-sectional study

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

Detection of fetal RHD-specific sequences in maternal plasma

Earliest gestational age for fetal sexing in cell-free maternal plasma

Does 17‐α‐hydroxyprogesterone caproate affect fetal biometry and birth weight in twin pregnancy?

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?

Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12)

Adverse obstetric outcome in low- and high-risk pregnancies: predictive value of maternal serum screening

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

Antiepileptic drug regimens and major congenital abnormalities in the offspring

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

Comparative genomic hybridization for cytogenetic evaluation of stillbirth

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

Does 17-[alpha]-hydroxyprogesterone caproate affect fetal biometry and birth weight in twin pregnancy?

Long-term Psychological Consequences of Pregnancy Termination for Fetal Abnormality: A Cross-sectional Study

SUCCESSFUL TREATMENT OF ACUTE PROMYELOCYTIC LEUKAEMIA WITH ALL‐TRANS‐RETINOIC‐ACID DURING LATE PREGNANCY

MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME 22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY 22

Comparison of platelet counts in first and second newborns of mothers with immune thrombocytopenic purpura

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