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Poly(3-hydroxyvalerate) depolymerase of Pseudomonas lemoignei.
Schöber U, Thiel C, Jendrossek D. Schöber U, et al. Among authors: thiel c. Appl Environ Microbiol. 2000 Apr;66(4):1385-92. doi: 10.1128/AEM.66.4.1385-1392.2000. Appl Environ Microbiol. 2000. PMID: 10742216 Free PMC article.
Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome.
Vasileiou G, Vergarajauregui S, Endele S, Popp B, Büttner C, Ekici AB, Gerard M, Bramswig NC, Albrecht B, Clayton-Smith J, Morton J, Tomkins S, Low K, Weber A, Wenzel M, Altmüller J, Li Y, Wollnik B, Hoganson G, Plona MR, Cho MT; Deciphering Developmental Disorders Study; Thiel CT, Lüdecke HJ, Strom TM, Calpena E, Wilkie AOM, Wieczorek D, Engel FB, Reis A. Vasileiou G, et al. Among authors: thiel ct. Am J Hum Genet. 2018 Mar 1;102(3):468-479. doi: 10.1016/j.ajhg.2018.01.014. Epub 2018 Feb 8. Am J Hum Genet. 2018. PMID: 29429572 Free PMC article.
Biallelic SEMA3A defects cause a novel type of syndromic short stature.
Hofmann K, Zweier M, Sticht H, Zweier C, Wittmann W, Hoyer J, Uebe S, van Haeringen A, Thiel CT, Ekici AB, Reis A, Rauch A. Hofmann K, et al. Among authors: thiel ct. Am J Med Genet A. 2013 Nov;161A(11):2880-9. doi: 10.1002/ajmg.a.36250. Epub 2013 Oct 3. Am J Med Genet A. 2013. PMID: 24124006
Exome Pool-Seq in neurodevelopmental disorders.
Popp B, Ekici AB, Thiel CT, Hoyer J, Wiesener A, Kraus C, Reis A, Zweier C. Popp B, et al. Among authors: thiel ct. Eur J Hum Genet. 2017 Dec;25(12):1364-1376. doi: 10.1038/s41431-017-0022-1. Epub 2017 Nov 20. Eur J Hum Genet. 2017. PMID: 29158550 Free PMC article.
Clinical and molecular delineation of spondylocostal dysostosis type 3.
Schuhmann S, Koller H, Sticht H, Kraus C, Krumbiegel M, Uebe S, Ekici AB, Reis A, Thiel CT. Schuhmann S, et al. Among authors: thiel ct. Clin Genet. 2021 Jun;99(6):851-852. doi: 10.1111/cge.13952. Epub 2021 Mar 16. Clin Genet. 2021. PMID: 33728697 No abstract available.
685 results