TY  - GEN
AU  - Smon,Andraz
AU  - Repic Lampret,Barbka
AU  - Groselj,Urh
AU  - Zerjav Tansek,Mojca
AU  - Kovac,Jernej
AU  - Perko,Dasa
AU  - Bertok,Sara
AU  - Battelino,Tadej
AU  - Trebusak Podkrajsek,Katarina
TI  - Next generation sequencing as a follow-up test in an expanded newborn screening programme
SN  - 1873-2933
PY  - 2018///0404
KW  - Acyl-CoA Dehydrogenase, Long-Chain
KW  - deficiency
KW  - Amino Acid Metabolism, Inborn Errors
KW  - diagnosis
KW  - Brain Diseases, Metabolic
KW  - Carbon-Carbon Ligases
KW  - Congenital Bone Marrow Failure Syndromes
KW  - Female
KW  - Follow-Up Studies
KW  - Glutaryl-CoA Dehydrogenase
KW  - High-Throughput Nucleotide Sequencing
KW  - methods
KW  - Humans
KW  - Infant, Newborn
KW  - Lipid Metabolism, Inborn Errors
KW  - Male
KW  - Metabolism, Inborn Errors
KW  - Mitochondrial Diseases
KW  - Muscular Diseases
KW  - Neonatal Screening
KW  - Pilot Projects
KW  - Slovenia
KW  - Tandem Mass Spectrometry
KW  - Urea Cycle Disorders, Inborn
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/j.clinbiochem.2017.10.016
ER  -