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Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Science (New York, N.Y.)|June 30, 2018
Heterogeneous to homogeneous melting transition visualized with ultrafast electron diffractionM Z Mo, Z Chen, R K Li, et al.
Nature|May 24, 2023
Observing the onset of pressure-driven K-shell delocalizationT Döppner, M Bethkenhagen, D Kraus, et al.
Nature Communications|March 13, 2021
Ultrafast multi-cycle terahertz measurements of the electrical conductivity in strongly excited solidsZ Chen, C B Curry, R Zhang, et al.
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