Canlyniadau Chwilio - H. Galjaard
- Dangos 1 - 20 canlyniadau o 31
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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 professiona... gan Adriana Kater‐Kuipers, Eline M. Bunnik, Inez D. de Beaufort, R. J. H. Galjaard
Cyhoeddwyd 2018Artigo -
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Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow gan Malgorzata I. Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert‐Jan H. Galjaard
Cyhoeddwyd 2011Artigo -
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Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature gan M. C. de Wit, Malgorzata I. Srebniak, L. Govaerts, Diane Van Opstal, R. J. H. Galjaard, Attie T. J. I. Go
Cyhoeddwyd 2013Revisão -
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Different Targets for the Fragile X-Related Proteins Revealed by Their Distinct Nuclear Localizations gan Filippo Tamanini, Carola Bontekoe, C.E. Bakker, Leontine van Unen, Burcu Anar, Rob Willemsen, Minoru Yoshida, H. Galjaard, Ben A. Oostra, A. T. Hoogeveen
Cyhoeddwyd 1999Artigo -
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Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples gan Diane Van Opstal, Marjan Boter, Daniëlle de Jong, Cardi van den Berg, Hennie T. Brüggenwirth, Hajo I. J. Wildschut, Annelies de Klein, Robert‐Jan H. Galjaard
Cyhoeddwyd 2008Artigo -
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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome gan Coleta Verheij, Cathy Bakker, Esther de Graaff, J. L. M. Keulemans, Rob Willemsen, Annemieke J.M.H. Verkerk, H. Galjaard, Arnold Reuser, A. T. Hoogeveen, Ben A. Oostra
Cyhoeddwyd 1993Artigo -
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Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique gan Rob Willemsen, Arie Smits, Serieta Mohkamsing, H. van Beerendonk, Anton de Haan, Bert de Vries, Ans van den Ouweland, Erik A. Sistermans, H. Galjaard, B. A. Oostra
Cyhoeddwyd 1997Artigo -
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The E6–AP Ubiquitin–Protein Ligase (<i>UBE3A</i>) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region gan James S. Sutcliffe, Yong‐hui Jiang, Robert‐Jan H. Galjaard, Toshinobu Matsuura, Ping Fang, Takeo Kubota, Susan L. Christian, Jan Bressler, B.M. Cattanach, David H. Ledbetter, Arthur L. Beaudet
Cyhoeddwyd 1997Carta -
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Defective deacetylation of histone 4 K12 in human oocytes is associated with advanced maternal age and chromosome misalignment gan I. M. van den Berg, C. Eleveld, M. van der Hoeven, Erwin Birnie, Eric A.P. Steegers, R. J. H. Galjaard, Joop S.E. Laven, J. Hikke van Doorninck
Cyhoeddwyd 2011Artigo -
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The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents’ Experiences gan Sanne Steen, Sam Riedijk, J. Verhagen‐Visser, L. Govaerts, Malgorzata I. Srebniak, Diane Van Opstal, Marieke Joosten, Maarten F. C. M. Knapen, Aad Tibben, Karin E. M. Diderich, R. J. H. Galjaard
Cyhoeddwyd 2016Artigo -
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False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review gan Diane Van Opstal, Malgorzata I. Srebniak, Joke Polak, Femke de Vries, Lutgarde Govaerts, Marieke Joosten, Attie T. J. I. Go, Maarten F. C. M. Knapen, Cardi van den Berg, Karin E. M. Diderich, Robert-Jan H. Galjaard
Cyhoeddwyd 2016Revisão
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Genetics
Medicine
Gene
Pregnancy
Fetus
Chromosome
Prenatal diagnosis
Obstetrics
Gynecology
Molecular biology
Aneuploidy
Pathology
Karyotype
Trisomy
Biochemistry
Computer science
Genetic testing
Internal medicine
Disease
Gene expression
Psychiatry
Amniocentesis
Cell biology
Chemistry
Environmental health
Enzyme
Family medicine
Fluorescence in situ hybridization
Genetic counseling