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Nine newly identified individuals refine the phenotype associated with MYT1L mutations.
Windheuser IC, Becker J, Cremer K, Hundertmark H, Yates LM, Mangold E, Peters S, Degenhardt F, Ludwig KU, Zink AM, Lessel D, Bierhals T, Herget T, Johannsen J, Denecke J, Wohlleber E, Strom TM, Wieczorek D, Bertoli M, Colombo R, Hempel M, Engels H. Windheuser IC, et al. Among authors: hundertmark h. Am J Med Genet A. 2020 May;182(5):1021-1031. doi: 10.1002/ajmg.a.61515. Epub 2020 Feb 17. Am J Med Genet A. 2020. PMID: 32065501
Nonlinear amplification of side-modes in frequency combs.
Probst RA, Steinmetz T, Wilken T, Hundertmark H, Stark SP, Wong GK, Russell PS, Hänsch TW, Holzwarth R, Udem T. Probst RA, et al. Among authors: hundertmark h. Opt Express. 2013 May 20;21(10):11670-87. doi: 10.1364/OE.21.011670. Opt Express. 2013. PMID: 23736390 Free article.
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