13 results on '"Galjaard, R J H"'
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2. Integrale geboortezorg – medisch-verloskundige en sociaal-maatschappelijke aandachtspunten
3. Benefit vs potential harm of genome‐wide prenatal cfDNA testing requires further investigation and should not be dismissed based on current data
4. Limits to the scope of non-invasive prenatal testing (NIPT): an analysis of the international ethical framework for prenatal screening and an interview study with Dutch professionals
5. Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
6. Prenatal and postnatal findings in small‐for‐gestational‐age fetuses without structural ultrasound anomalies at 18–24 weeks
7. Identification of Associated Genes and Diseases in Patients With Congenital Upper Limb Anomalies
8. The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents’ Experiences
9. Whole-genome array as a first-line cytogenetic test in prenatal diagnosis
10. Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature
11. Omphalocele: comparison of outcome following prenatal or postnatal diagnosis
12. False positive FISH diagnosis of monosomy X in uncultured amniotic fluid cells due to a chromosome Y deletion
13. First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis
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