Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities

BACKGROUND: We have investigated whether replacing conventional karyotyping by SNP array analysis in cases of foetal ultrasound abnormalities would increase the diagnostic yield and speed of prenatal diagnosis in clinical practice. FINDINGS/RESULTS: From May 2009 till June 2011 we performed HumanCyt...

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Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2012
Matèries:
Short Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3328283/
https://ncbi.nlm.nih.gov/pubmed/22413963
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-5-14
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