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Page 1
Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome.
Sheikhzadeh S, Kade C, Keyser B, Stuhrmann M, Arslan-Kirchner M, Rybczynski M, Bernhardt AM, Habermann CR, Hillebrand M, Mir T, Robinson PN, Berger J, Detter C, Blankenberg S, Schmidtke J, von Kodolitsch Y. Sheikhzadeh S, et al. Among authors: stuhrmann m. Clin Genet. 2012 Sep;82(3):240-7. doi: 10.1111/j.1399-0004.2011.01771.x. Epub 2011 Oct 5. Clin Genet. 2012. PMID: 21883168
Augmentation index and the evolution of aortic disease in marfan-like syndromes.
Mortensen K, Baulmann J, Rybczynski M, Sheikhzadeh S, Aydin MA, Treede H, Dombrowski E, Kühne K, Peitsmeier P, Habermann CR, Robinson PN, Stuhrmann M, Berger J, Meinertz T, von Kodolitsch Y. Mortensen K, et al. Among authors: stuhrmann m. Am J Hypertens. 2010 Jul;23(7):716-24. doi: 10.1038/ajh.2010.78. Epub 2010 Apr 15. Am J Hypertens. 2010. PMID: 20395939
Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome.
Wessels K, Bohnhorst B, Luhmer I, Morlot S, Bohring A, Jonasson J, Epplen JT, Gadzicki D, Glaser S, Göhring G, Mälzer M, Hein A, Arslan-Kirchner M, Stuhrmann M, Schmidtke J, Pabst B. Wessels K, et al. Among authors: stuhrmann m. Eur J Med Genet. 2010 Sep-Oct;53(5):280-5. doi: 10.1016/j.ejmg.2010.07.002. Epub 2010 Jul 30. Eur J Med Genet. 2010. PMID: 20624498
PCR-based mutation analysis in cystic fibrosis.
Stuhrmann M, Schmidtke J. Stuhrmann M, et al. Ann Med. 1992 Jun;24(3):183-5. doi: 10.3109/07853899209147818. Ann Med. 1992. PMID: 1627313 Free article. No abstract available.
142 results