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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

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Absolute first trimester cell-free DNA levels and their associations with adverse pregnancy outcomes

Prenatal diagnosis, 2016-12, Vol.36 (12), p.1104-1111

2016

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A faint companion around CrA-9: protoplanet or obscured binary?

Monthly notices of the Royal Astronomical Society, 2021-04, Vol.502 (4), p.6117-6139

2021

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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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Corporate social responsibility reporting: A comprehensive picture?

Accounting forum, 2011-09, Vol.35 (3), p.187-204

2011

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Women with symptoms of a urinary tract infection but a negative urine culture: PCR-based quantification of Escherichia coli suggests infection in most cases

Clinical microbiology and infection, 2017-09, Vol.23 (9), p.647-652

2017

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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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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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High-contrast imaging of HD 163296 with the Keck/NIRC2 L′-band vortex coronograph

Monthly notices of the Royal Astronomical Society, 2018-09, Vol.479 (2), p.1505-1513

2018

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Non‐invasive prenatal detection of achondroplasia in size‐fractionated cell‐free DNA by MALDI‐TOF MS assay

Prenatal diagnosis, 2007-01, Vol.27 (1), p.11-17

2007

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

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

2013

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Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma-case report

Prenatal diagnosis, 2004-11, Vol.24 (11), p.896-898

2004

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Use of bi-allelic insertion/deletion polymorphisms as a positive control for fetal genotyping in maternal blood: first clinical experience

Annals of the New York Academy of Sciences, 2006-09, Vol.1075 (1), p.123-129

2006

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Self-medication of regular headache: a community pharmacy-based survey

European journal of neurology, 2012-08, Vol.19 (8), p.1093-1099

2012

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Comprehensive survey of developmental genes in the pea aphid, Acyrthosiphon pisum: frequent lineage-specific duplications and losses of developmental genes

Insect molecular biology, 2010-03, Vol.19 (s2), p.47-62

2010

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Six uneventful pregnancy outcomes in an extended vascular Ehlers–Danlos syndrome family

American journal of medical genetics. Part A, 2017-02, Vol.173 (2), p.519-523

2017

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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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Psychological consequences of termination of pregnancy for fetal anomaly: similarities and differences between partners

Prenatal diagnosis, 2005-12, Vol.25 (13), p.1226-1233

2005

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Recovery of upper limb function after axillary dissection

Journal of surgical oncology, 2003-08, Vol.83 (4), p.204-211

2003

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Harmonizing and improving European education in prescribing: An overview of digital educational resources used in clinical pharmacology and therapeutics

British journal of clinical pharmacology, 2021-03, Vol.87 (3), p.1001-1011

2021

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Absolute first trimester cell-free DNA levels and their associations with adverse pregnancy outcomes: Cell-free DNA levels and pregnancy outcomes

Prenatal diagnosis, 2016-12, Vol.36 (12), p.1104-1111

2016

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DNA attachment to nanocrystalline diamond films

Physica status solidi. A, Applications and materials science, 2005-09, Vol.202 (11), p.2212-2216

2005

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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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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

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The applicability of different PCR-based methods for fetal RHD and K1 genotyping: a prospective study

Prenatal diagnosis, 2000-06, Vol.20 (6), p.453-458

2000

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

Absolute first trimester cell-free DNA levels and their associations with adverse pregnancy outcomes

A faint companion around CrA-9: protoplanet or obscured binary?

Noninvasive fetal genotyping of human platelet antigen‐1a

Corporate social responsibility reporting: A comprehensive picture?

Women with symptoms of a urinary tract infection but a negative urine culture: PCR-based quantification of Escherichia coli suggests infection in most cases

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

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

High-contrast imaging of HD 163296 with the Keck/NIRC2 L′-band vortex coronograph

Non‐invasive prenatal detection of achondroplasia in size‐fractionated cell‐free DNA by MALDI‐TOF MS assay

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

Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma-case report

Use of bi-allelic insertion/deletion polymorphisms as a positive control for fetal genotyping in maternal blood: first clinical experience

Self-medication of regular headache: a community pharmacy-based survey

Comprehensive survey of developmental genes in the pea aphid, Acyrthosiphon pisum: frequent lineage-specific duplications and losses of developmental genes

Six uneventful pregnancy outcomes in an extended vascular Ehlers–Danlos syndrome family

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

Psychological consequences of termination of pregnancy for fetal anomaly: similarities and differences between partners

Recovery of upper limb function after axillary dissection

Harmonizing and improving European education in prescribing: An overview of digital educational resources used in clinical pharmacology and therapeutics

Absolute first trimester cell-free DNA levels and their associations with adverse pregnancy outcomes: Cell-free DNA levels and pregnancy outcomes

DNA attachment to nanocrystalline diamond films

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

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

The applicability of different PCR-based methods for fetal RHD and K1 genotyping: a prospective study

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