Publications by authors named "Moritz Meins"

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The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
Miriam Gordillo, Hugo Vega, Alison H Trainer, Fajian Hou, Norio Sakai, Moritz Meins

Hum Mol Genet· July 2008

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Severe Guillain-Barré syndrome associated with chromosome 17p11.2-12 duplication.
Christoph Münch, Jörg T Epplen, Moritz Meins, Robert Meyer, Jörg R Weber

Muscle Nerve· February 2008

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Mice deficient for RNA-binding protein brunol1 show reduction of spermatogenesis but are fertile.
Arvind Dev, Karim Nayernia, Moritz Meins, Ibrahim Adham, Franco Lacone

Mol Reprod Dev· November 2007

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Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).
Kathrin Engelfried, Matthias Vorgerd, Michaela Hagedorn, Gerhard Haas, Jürgen Gilles, Moritz Meins

BMC Med Genet· June 2006

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Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects.
René Gödde, Denis-Amer Akkad, Larissa Arning, Gabriele Dekomien, Julia Herchenbach, Moritz Meins

Electrophoresis· March 2006

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Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
Moritz Meins, Javad Karimzad Hagh, Fritz Gerresheim, Elisabeth Einhoff, Heidi Olschewski

Am J Med Genet A· January 2005

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A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?
Knut Brockmann, Moritz Meins, Angelika Taubert, Ralf Trappe, Martin Grond

Eur Neurol· November 2003

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Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease.
Knut Brockmann, Peter Dechent, Moritz Meins, Mechthild Haupt, Jürgen Sperner

J Neurol· March 2003

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Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.
Barbara Zoll, Lars Petersen, Katrin Lange, Peter Gabriel, Christiane Kiese-Himmel, Moritz Meins

Hum Mutat· January 2003

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