Výsledky vyhledávání - Ida Vogel

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  1. 1
    Biomarkers for the prediction of preterm delivery

    Biomarkers for the prediction of preterm delivery Autor Ida Vogel, Poul Thorsen, Allison E. Curry, Puk Sandager, Niels Uldbjerg

    Vydáno 2005
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  2. 2
    Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study

    Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study Autor Jens Langhoff‐Roos, Ulrik Schiøler Kesmodel, Bo Jacobsson, Steen Rasmussen, Ida Vogel

    Vydáno 2006
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  3. 3
    Chromosomal microarray in fetuses with increased nuchal translucency

    Chromosomal microarray in fetuses with increased nuchal translucency Autor Ida Charlotte Bay Lund, Rikke Christensen, Olav Bjørn Petersen, Ida Vogel, Else Marie Vestergaard

    Vydáno 2014
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  4. 4
    Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population‐based combined first‐trimester screening program

    Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population‐based combined first‐trimester screening program Autor Ida Vogel, Olav Bjørn Petersen, Rikke Christensen, Jon Hyett, Stina Lou, Else Marie Vestergaard

    Vydáno 2017
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  5. 5
    Experiences and expectations in the first trimester of pregnancy: a qualitative study

    Experiences and expectations in the first trimester of pregnancy: a qualitative study Autor Stina Lou, Michal Frumer, Mette Mørup Schlütter, Olav Bjørn Petersen, Ida Vogel, Camilla Palmhøj Nielsen

    Vydáno 2017
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  6. 6
    Fetal Cells in Maternal Blood For Prenatal Diagnosis: A Love Story Rekindled

    Fetal Cells in Maternal Blood For Prenatal Diagnosis: A Love Story Rekindled Autor Ripudaman Singh, Lotte Hatt, Katarina Ravn, Ida Vogel, Olav Bjørn Petersen, Niels Uldbjerg, Palle Schelde

    Vydáno 2017
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  7. 7
    Implementation of exome sequencing in fetal diagnostics—Data and experiences from a tertiary center in Denmark

    Implementation of exome sequencing in fetal diagnostics—Data and experiences from a tertiary center in Denmark Autor Naja Becher, Lotte Andreasen, Puk Sandager, Stina Lou, Olav Bjørn Petersen, Rikke Christensen, Ida Vogel

    Vydáno 2020
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  8. 8
    National screening guidelines and developments in prenatal diagnoses and live births of Down syndrome in 1973–2016 in Denmark

    National screening guidelines and developments in prenatal diagnoses and live births of Down syndrome in 1973–2016 in Denmark Autor Stina Lou, Olav Bjørn Petersen, Finn Stener Jørgensen, Ida Charlotte Bay Lund, Susanne Kjærgaard, Ida Vogel

    Vydáno 2017
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  9. 9
    Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study

    Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study Autor Ellen Hollands Steffensen, Anne Skakkebæk, Kasper Gadsbøll, Olav Bjørn Petersen, Thomas Westover, Heather Strange, Ida Vogel

    Vydáno 2023
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  10. 10
    Increased nuchal translucency thickness and normal chromosomal microarray: Danish nationwide cohort study

    Increased nuchal translucency thickness and normal chromosomal microarray: Danish nationwide cohort study Autor Kasper Gadsbøll, Nis Brix, Puk Sandager, Olav Bjørn Petersen, Athena P. Souka, K. H. Nicolaides, Ida Vogel

    Vydáno 2025
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  11. 11
    Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

    Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype Autor Tak Yeung Leung, Ida Vogel, Tze Kin Lau, Wilson Chong, Jon Hyett, Olav Bjørn Petersen, Kwong Wai Choy

    Vydáno 2011
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  12. 12
    Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation

    Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation Autor Kasper Gadsbøll, Olav Bjørn Petersen, Vincent Gâtinois, Heather Strange, Bo Jacobsson, Ronald J. Wapner, Joris Vermeesch, Ida Vogel

    Vydáno 2020
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  13. 13
    Maternal age and the risk of fetal aneuploidy: A nationwide cohort study of more than 500 000 singleton pregnancies in Denmark from 2008 to 2017

    Maternal age and the risk of fetal aneuploidy: A nationwide cohort study of more than 500 000 singleton pregnancies in Denmark from 2008 to 2017 Autor Line Elmerdahl Frederiksen, Sofie Møller Ølgaard, Laura Roos, Olav Bjørn Petersen, Line Rode, Tanja Schlaikjær Hartwig, C. K. Ekelund, Ida Vogel

    Vydáno 2023
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  14. 14
    Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly

    Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly Autor Rikke S. Møller, Sabine Kübart, Maria Hoeltzenbein, Babett Heye, Ida Vogel, Christian Pilebæk Hansen, Corinna Menzel, Reinhard Ullmann, Niels Tommerup, Hans‐Hilger Ropers, Zeynep Tümer, Vera M. Kalscheuer

    Vydáno 2008
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  15. 15
    Non‐Invasive Prenatal Testing by Cell‐Free <scp>DNA</scp> (<scp>cfNIPT</scp>) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal Outcomes

    Non‐Invasive Prenatal Testing by Cell‐Free <scp>DNA</scp> (<scp>cfNIPT</scp>) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal O... Autor Ivonne Bedei, Johanna Bruder, Ida Charlotte Bay Lund, Simon Horsholt Thomsen, Ida Vogel, Andréa Trevas Maciel‐Guerra, Francisco Álvarez‐Nava, Melissa Crenshaw, R Axt-Fliedner, Claus Højbjerg Gravholt, Anne Skakkebæk

    Vydáno 2025
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  16. 16
    Nuchal translucency of 3.0‐3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review

    Nuchal translucency of 3.0‐3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review Autor Olav Bjørn Petersen, Eric E. Smith, Diane Van Opstal, Marike Polak, Maarten F. C. M. Knapen, Karin E. M. Diderich, Caterina M. Bilardo, Lidia R. Arends, Ida Vogel, Malgorzata I. Srebniak

    Vydáno 2020
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  17. 17
    Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome

    Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome Autor Karin Huijsdens–van Amsterdam, Lieve Page‐Christiaens, Nicola Flowers, Michael Bonifacio, Katie M Battese Ellis, Ida Vogel, Else Marie Vestergaard, Javier Miguelez, Mário Henrique Burlacchini de Carvalho, Erik A. Sistermans, Mark D. Pertile

    Vydáno 2018
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  18. 18
    Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes

    Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes Autor Robert Schöpflin, Uirá Souto Melo, Hossein Moeinzadeh, David N. Heller, Verena Laupert, Jakob Hertzberg, Manuel Holtgrewe, Nico Alavi, Marius-Konstantin Klever, Julius Jungnitsch, Emel Comak, Seval Türkmen, Denise Horn, Yannis Duffourd, Laurence Faivre, Patrick Callier, Damien Sanlaville, Orsetta Zuffardi, Romano Tenconi, Nehir Edibe Kurtas, Sabrina Giglio, Bettina Prager, Anna Latos‐Bieleńska, Ida Vogel, Merete Bugge, Niels Tommerup, Malte Spielmann, Antonio Vitobello, Vera M. Kalscheuer, Martin Vingron, Stefan Mundlos

    Vydáno 2022
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  19. 19
    Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals

    Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals Autor Melissa Hill, Jo-Ann Johnson, Sylvie Langlois, Hyun Lee, Stephanie Winsor, Brigid Dineley, Marisa Horniachek, Faustina Lalatta, Luisa Ronzoni, Angela N. Barrett, Henna V. Advani, Mahesh Choolani, Ron Rabinowitz, Eva Pajkrt, Rachèl V. van Schendel, Lidewij Henneman, Wieke Rommers, Caterina M. Bilardo, Paula Rendeiro, Maria João Rodrigues Ferreira Ribeiro, José Rocha, Ida Charlotte Bay Lund, Olav Bjørn Petersen, Naja Becher, Ida Vogel, Vigdís Stefànsdóttir, Sigrún Ingvarsdóttir, Helga Gottfreðsdóttir, Stephen Morris, Lyn S. Chitty

    Vydáno 2015
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  20. 20
    Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

    Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders Autor Holly A.F. Stessman, Marjolein H. Willemsen, Michaela Fencková, Osnat Penn, Alexander Hoischen, Bo Xiong, Tianyun Wang, Kendra Hoekzema, Laura Vives, Ida Vogel, Han G. Brunner, Ineke van der Burgt, Charlotte W. Ockeloen, Janneke Schuurs-Hoeijmakers, Jolien S. Klein Wassink‐Ruiter, Connie T. R. M. Stumpel, Servi J.C. Stevens, Hans S.H. Vles, Carlo Marcelis, Hans van Bokhoven, Vincent Cantagrel, Laurence Colleaux, Michaël Nicouleau, Stanislas Lyonnet, Raphael A. Bernier, Jennifer Gerdts, Bradley P. Coe, Corrado Romano, A Alberti, Lucia Grillo, Carmela Scuderi, Magnus Nordenskjöld, Malin Kvarnung, Hui Guo, Kun Xia, Amélie Piton, Bénédicte Gérard, David Geneviève, Bruno Delobel, Daphné Lehalle, Laurence Perrin, Fabienne Prieur, Julien Thévenon, Jozef Gécz, Marie Shaw, Rolph Pfundt, Boris Keren, Aurélia Jacquette, Annette Schenck, Evan E. Eichler, Tjitske Kleefstra

    Vydáno 2016
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