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Genetic variants of the promoter of the heme oxygenase-1 gene and their influence on cardiovascular disease (the Ludwigshafen Risk and Cardiovascular Health study).
BMC Med Genet. 2009 Apr 23;10:36. doi: 10.1186/1471-2350-10-36.
BMC Med Genet. 2009.
PMID: 19389234
Free PMC article.
Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene.
Birkenhäger R, Lüblinghoff N, Prera E, Schild C, Aschendorff A, Arndt S.
Birkenhäger R, et al. Among authors: lublinghoff n.
Am J Med Genet A. 2010 Jul;152A(7):1798-802. doi: 10.1002/ajmg.a.33464.
Am J Med Genet A. 2010.
PMID: 20583176
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Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss.
Schild C, Prera E, Lüblinghoff N, Arndt S, Aschendorff A, Birkenhäger R.
Schild C, et al. Among authors: lublinghoff n.
Otol Neurotol. 2011 Jun;32(4):690-4. doi: 10.1097/MAO.0b013e318210b749.
Otol Neurotol. 2011.
PMID: 21555964
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[Coil migration after neuroradiologic intervention due to hemorrhage in oropharyngeal carcinoma].
Lüblinghoff N, Weerda N, Hader C, Laszig R.
Lüblinghoff N, et al.
Laryngorhinootologie. 2013 Mar;92(3):184-5. doi: 10.1055/s-0032-1327580. Epub 2012 Oct 9.
Laryngorhinootologie. 2013.
PMID: 23047177
German.
No abstract available.
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