Publications by authors named "Michael Lingen"

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Continuing role for classical cytogenetics: Case report of a boy with ring syndrome caused by complete ring chromosome 4 and review of literature.
Anna Lena Burgemeister, Eva Daumiller, Ilona Dietze-Armana, Christine Klett, Clemens Freiberg, Michael Lingen

Am J Med Genet A· March 2017

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Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study.
Sarah Wente, Simone Schröder, Johannes Buckard, Hans-Martin Büttel, Florian von Deimling, Michael Lingen

Orphanet J Rare Dis· July 2016

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Microduplication of 3p26.3 in nonsyndromic intellectual disability indicates an important role of CHL1 for normal cognitive function.
Moneef Shoukier, Sigrid Fuchs, Eva Schwaibold, Michael Lingen, Jutta Gärtner

Neuropediatrics· October 2013

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A de novo interstitial deletion of 2p23.3-24.3 in a boy presenting with intellectual disability, overgrowth, dysmorphic features, skeletal myopathy, dilated cardiomyopathy.
Moneef Shoukier, Julia Schröder, Barbara Zoll, Peter Burfeind, Clemens Freiberg, Michael Lingen

Am J Med Genet A· February 2012

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