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Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects.
Electrophoresis. 2006 Mar;27(5-6):939-46. doi: 10.1002/elps.200500675.
Electrophoresis. 2006.
PMID: 16470775
Review.
The transcription factor-like nuclear regulator (TFNR) contains a novel 55-amino-acid motif repeated nine times and maps closely to SMN1.
Kelter AR, Herchenbach J, Wirth B.
Kelter AR, et al. Among authors: herchenbach j.
Genomics. 2000 Dec 15;70(3):315-26. doi: 10.1006/geno.2000.6396.
Genomics. 2000.
PMID: 11161782
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Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome.
Meins M, Lehmann J, Gerresheim F, Herchenbach J, Hagedorn M, Hameister K, Epplen JT.
Meins M, et al. Among authors: herchenbach j.
J Med Genet. 2005 Feb;42(2):e12. doi: 10.1136/jmg.2004.023804.
J Med Genet. 2005.
PMID: 15689435
Free PMC article.
No abstract available.
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Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.
Hartmann H, Herchenbach J, Stephani U, Ledaal P, Donnerstag F, Lücke T, Das AM, Christen HJ, Hagedorn M, Meins M.
Hartmann H, et al. Among authors: herchenbach j.
Neuropediatrics. 2007 Jun;38(3):143-7. doi: 10.1055/s-2007-985902.
Neuropediatrics. 2007.
PMID: 17985264
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