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Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
Orphanet J Rare Dis. 2015 Apr 2;10:40. doi: 10.1186/s13023-015-0254-5.
Orphanet J Rare Dis. 2015.
PMID: 25887401
Free PMC article.
Two-year neurodevelopmental outcome in extremely preterm-born children: The Austrian Preterm Outcome Study Group.
Kiechl-Kohlendorfer U, Simma B, Berger A, Urlesberger B, Wald M, Haiden N, Fuiko R, Ndayisaba JP; Austrian Preterm Outcome Study Group.
Kiechl-Kohlendorfer U, et al.
Acta Paediatr. 2024 Jun;113(6):1278-1287. doi: 10.1111/apa.17187. Epub 2024 Mar 3.
Acta Paediatr. 2024.
PMID: 38433292
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