Genome-wide scans using archived neonatal dried blood spot samples

被引：0
|
作者：
Mads V Hollegaard
Jonas Grauholm
Anders Børglum
Mette Nyegaard
Bent Nørgaard-Pedersen
Torben Ørntoft
Preben B Mortensen
Carsten Wiuf
Ole Mors
Michael Didriksen
Poul Thorsen
David M Hougaard
机构：
[1] Statens Serum Institut,Section of Neonatal Screening and Hormones
[2] University of Aarhus,Department of Epidemiology
[3] AROS Applied Biotechnology A/S,Institute of Human Genetics
[4] University of Aarhus,Department of Clinical Biochemistry
[5] Skejby Sygehus,The National Centre for Register Based Research
[6] University of Aarhus,Bioinformatics Research Center
[7] University of Aarhus,Centre for Psychiatric Research
[8] Aarhus University Hospital Risskov,Department of Epidemiology, Rollins School of Public Health
[9] Lundbeck A/S,undefined
[10] Emory University,undefined
来源：
BMC Genomics | / 10卷
关键词：
Single Nucleotide Polymorphism; Newborn Screening Program; Cluster File; gDNA Sample; Input gDNA;
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