受强制性开放获取政策约束的文章 - Thierry Nouspikel了解详情
可在其他位置公开访问的文章：4 篇
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients
S Laurent, C Gehrig, T Nouspikel, SS Amr, A Oza, E Murphy, A Vannier, ...
Human mutation 42 (4), 373-377, 2021
强制性开放获取政策： US National Institutes of Health
Precision medicine in diabetes: a non‐invasive prenatal diagnostic test for the determination of fetal glucokinase mutations
T Nouspikel, JL Blouin, JJ Puder, B Köhler Ballan, VM Schwitzgebel
Journal of Diabetes Investigation 13 (2), 256-261, 2022
强制性开放获取政策： Swiss National Science Foundation
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant
R Ricciardiello, G Forleo, L Cipolla, G van Winckel, C Marconi, ...
Scientific Reports 14 (1), 1117, 2024
强制性开放获取政策： Swiss National Science Foundation, AIRC Foundation for Cancer Research in Italy
Attenuated nucleotide excision repair leads to mutagenesis in cancer cells
T Nouspikel
Future Oncology 7 (12), 1361-1363, 2011
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health
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