(Q50545746)

15 March 2018

title

Storage policies and use of the Danish Newborn Screening Biobank. (English)

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15 March 2018

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B Nørgaard-Pedersen

1

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15 March 2018

D M Hougaard

series ordinal

2

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15 March 2018

publication date

12 July 2007

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15 March 2018

Journal of Inherited Metabolic Disease

published in

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15 March 2018

volume

30

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15 March 2018

issue

4

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15 March 2018

page(s)

530-536

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15 March 2018

https://scigraph.springernature.com/pub.10.1007/s10545-007-0631-x

exact match

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cites work

Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: a population-based case-control study in Denmark, 1991-1994.

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Crossref

https://api.crossref.org/works/10.1007%2FS10545-007-0631-X

Neonatal screening by DNA microarray: spots and chips

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Crossref

https://api.crossref.org/works/10.1007%2FS10545-007-0631-X

[Neonatal screening in Denmark. Status and future perspectives]

21 January 2018

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12 December 2020

Simultaneous quantitation of diphtheria and tetanus antibodies by double antigen, time-resolved fluorescence immunoassay

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Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic Services.

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The Arg506Gln mutation (FV Leiden) among a cohort of 4188 unselected Danish newborns

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Risk factors for parvovirus B19 infection in pregnancy.

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12 December 2020

Storage and use of residual dried blood spots.

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A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations

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Incidence of the apolipoprotein B-3500 mutation in Denmark.

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Diagnosis of Zellweger syndrome by analysis of very long-chain fatty acids in stored blood spots collected at neonatal screening

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The frequency of an inactivating point mutation (566C-->T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry

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Accuracy of multiplexed Illumina platform-based single-nucleotide polymorphism genotyping compared between genomic and whole genome amplified DNA collected from multiple sources

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The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome

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The Danish National Birth Cohort--its background, structure and aim.

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Early manifestations of the carbohydrate-deficient glycoprotein syndrome.

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Feasibility of neonatal screening for toxoplasma infection in the absence of prenatal treatment. Danish Congenital Toxoplasmosis Study Group .

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Whole Genome Amplification and Genetic Analysis after Extraction of Proteins from Dried Blood Spots

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Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

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Neonatal screening for congenital toxoplasmosis in Denmark: presentation of the design of a prospective study

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Newborn screening for lysosomal storage disorders: clinical evaluation of a two-tier strategy

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12 December 2020

Biological specimen banks in neonatal screening

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Determination of a common genetic variant of luteinizing hormone using DNA hybridization and immunoassays

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Carnitine transporter and holocarboxylase synthetase deficiencies in The Faroe Islands.

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Toxoplasma gondii as a risk factor for early-onset schizophrenia: analysis of filter paper blood samples obtained at birth

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Cholestasis Familiaris Groenlandica/Byler-like disease in Greenland--a population study

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Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems.

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Type 1 diabetes risk analysis on dried blood spot samples from population-based newborns: design and feasibility of an unselected case-control study

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Storage and use of residual dried blood spots from state newborn screening programs

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Simultaneous measurement of 25 inflammatory markers and neurotrophins in neonatal dried blood spots by immunoassay with xMAP technology

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12 December 2020

Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism.

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Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

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12 December 2020

10.1007/S10545-007-0631-X

Identifiers

DOI

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15 March 2018

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15 March 2018