Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8166
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities ; volume:5 ; number:1 ; day:13 ; month:3 ; year:2012 ; pages:1-4 ; date:12.2012
Molecular cytogenetics ; 5, Heft 1 (13.3.2012), 1-4, 12.2012
- Creator
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Srebniak, Malgorzata I.
Boter, Marjan
Oudesluijs, Gretel O.
Cohen-Overbeek, Titia
Govaerts, Lutgarde CP
Diderich, Karin EM
Oegema, Renske
Knapen, Maarten FCM
van de Laar, Ingrid MBH
Joosten, Marieke
Van Opstal, Diane
Galjaard, Robert-Jan H.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/1755-8166-5-14
- URN
-
urn:nbn:de:101:1-2019090220563775316121
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 12:27 PM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Srebniak, Malgorzata I.
- Boter, Marjan
- Oudesluijs, Gretel O.
- Cohen-Overbeek, Titia
- Govaerts, Lutgarde CP
- Diderich, Karin EM
- Oegema, Renske
- Knapen, Maarten FCM
- van de Laar, Ingrid MBH
- Joosten, Marieke
- Van Opstal, Diane
- Galjaard, Robert-Jan H.
- SpringerLink (Online service)
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Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
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Exploring general practitioners' experience of informing women about prenatal screening tests for foetal abnormalities: A qualitative focus group study
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Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
SAQC: SNP Array Quality Control
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Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities
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