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1
An incidental finding of maternal multiple myeloma by non invasive prenatal testing
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Article
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An incidental finding of maternal multiple myeloma by non invasive prenatal testing

Prenatal diagnosis, 2017-12, Vol.37 (12), p.1257-1260 [Peer Reviewed Journal]

Attribution - NonCommercial - NoDerivatives ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5168 ;PMID: 29023902

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2
Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia
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Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia

Prenatal diagnosis, 2016-05, Vol.36 (5), p.397-406 [Peer Reviewed Journal]

2016 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4790 ;PMID: 26850935

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3
Feticide in second‐ and third‐trimester termination of pregnancy for fetal anomalies: Results of a national survey
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Feticide in second‐ and third‐trimester termination of pregnancy for fetal anomalies: Results of a national survey

Prenatal diagnosis, 2019-12, Vol.39 (13), p.1269-1272 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5594

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4
Performance of diagnostic ultrasound to identify causes of hydramnios
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Article
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Performance of diagnostic ultrasound to identify causes of hydramnios

Prenatal diagnosis, 2021-01, Vol.41 (1), p.111-122 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5825 ;PMID: 32920845

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5
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
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Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?

Prenatal diagnosis, 2019-10, Vol.39 (11), p.986-992 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5518 ;PMID: 31273809

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6
Information and decision-making process for selective termination of dichorionic pregnancies: some French obstetricians' points of view
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Article
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Information and decision-making process for selective termination of dichorionic pregnancies: some French obstetricians' points of view

Prenatal diagnosis, 2009-01, Vol.29 (1), p.89-94 [Peer Reviewed Journal]

Copyright © 2008 John Wiley & Sons, Ltd. ;2009 INIST-CNRS ;Copyright (c) 2008 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2174 ;PMID: 19101926 ;CODEN: PRDIDM

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7
Fetal anomalies associated with HNF1B mutations: report of 20 autopsy cases
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Article
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Fetal anomalies associated with HNF1B mutations: report of 20 autopsy cases

Prenatal diagnosis, 2016-08, Vol.36 (8), p.744-751 [Peer Reviewed Journal]

2016 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4858 ;PMID: 27297286

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8
How important is consent in maternal serum screening for Down syndrome in France? Information and consent evaluation in maternal serum screening for Down syndrome: a French study
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Article
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How important is consent in maternal serum screening for Down syndrome in France? Information and consent evaluation in maternal serum screening for Down syndrome: a French study

Prenat Diagn, 2007-03, Vol.27 (3), p.197-205 [Peer Reviewed Journal]

Copyright © 2007 John Wiley & Sons, Ltd. ;2007 INIST-CNRS ;Copyright (c) 2007 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1656 ;PMID: 17238219 ;CODEN: PRDIDM

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9
Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12-year population-based study
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Article
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Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12-year population-based study

Prenatal diagnosis, 2008-11, Vol.28 (11), p.1016-1022 [Peer Reviewed Journal]

Copyright © 2008 John Wiley & Sons, Ltd. ;2008 INIST-CNRS ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2113 ;PMID: 18925579 ;CODEN: PRDIDM

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10
Clinical and socioeconomic predictors of pregnancy termination for fetuses with congenital heart defects: a population-based evaluation: Pregnancy termination for fetuses with CHD
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Article
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Clinical and socioeconomic predictors of pregnancy termination for fetuses with congenital heart defects: a population-based evaluation: Pregnancy termination for fetuses with CHD

Prenatal diagnosis, 2013-02, Vol.33 (2), p.179-86 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4043 ;PMID: 23307581

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11
Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome
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Article
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Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome

Prenatal diagnosis, 2010-11, Vol.30 (11), p.1072-1078 [Peer Reviewed Journal]

Copyright © 2010 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2613 ;PMID: 20842625 ;CODEN: PRDIDM

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