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High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors.
Mol Genet Genomic Med. 2014 Mar;2(2):176-85. doi: 10.1002/mgg3.60. Epub 2014 Jan 14.
Mol Genet Genomic Med. 2014.
PMID: 24689081
Free PMC article.
[Gomez-López-Hernández-Syndrome].
Lettau M, Munk RD, Munk-Schulenburg S.
Lettau M, et al. Among authors: munk schulenburg s.
Rofo. 2013 Jul;185(7):662-3. doi: 10.1055/s-0033-1335027. Epub 2013 Mar 14.
Rofo. 2013.
PMID: 23494500
Free article.
German.
No abstract available.
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Actual management of patients with familial ascending aortic aneurysms and type-A aortic dissections.
Weigang E, Chang XC, Munk-Schulenburg S, Richter H, von Samson P, Goebel H, Frydrychowicz A, Geibel A, Ammann S, Schwering L, Brunner T, Severin T, Czerny M, Beyersdorf F.
Weigang E, et al. Among authors: munk schulenburg s.
Thorac Cardiovasc Surg. 2007 Feb;55(1):19-23. doi: 10.1055/s-2006-924575.
Thorac Cardiovasc Surg. 2007.
PMID: 17285469
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SALL1 mutations in sporadic Townes-Brocks syndrome are of predominantly paternal origin without obvious paternal age effect.
Böhm J, Munk-Schulenburg S, Felscher S, Kohlhase J.
Böhm J, et al. Among authors: munk schulenburg s.
Am J Med Genet A. 2006 Sep 15;140(18):1904-8. doi: 10.1002/ajmg.a.31383.
Am J Med Genet A. 2006.
PMID: 16892410
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