Publications by authors named "Ina Goehring"

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Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrum.
Diana Zahnleiter, Udo Trautmann, Arif B Ekici, Ina Goehring, André Reis

Eur J Med Genet· December 2011

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Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice.
Michael Kraft, Ion Cristian Cirstea, Anne Kathrin Voss, Tim Thomas, Ina Goehring

J Clin Invest· September 2011

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De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation.
Ute Grasshoff, Michael Bonin, Ina Goehring, Arif Ekici, Andreas Dufke

Eur J Hum Genet· May 2011

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