Maarten FCM Knapen

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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. From May 2009 till June 2011 we performed HumanCytoSNP-12 array (HCS) ( http://www.Illumina.com ) analysis in 207 cases of foetal(More)
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