Publications by authors named "H Hundertmark"

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Next-generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen-de Vries syndrome.
Fabian Brand, Aswinkumar Vijayananth, Tzung-Chien Hsieh, Axel Schmidt, Sophia Peters, Hela Hundertmark

Hum Mutat· November 2022

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Occurrence of a paroxysmal nocturnal hemoglobinuria clone in an essential thrombocythemia: a link between and .
Alexej Knaus, François Vergez, Cédric Garcia, Hartmut Engels, Hela Hundertmark

Haematologica· August 2022

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Nine newly identified individuals refine the phenotype associated with MYT1L mutations.
Isabelle C Windheuser, Jessica Becker, Kirsten Cremer, Hela Hundertmark, Laura M Yates

Am J Med Genet A· May 2020

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De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies.
Daniel Fritzen, Alma Kuechler, Mona Grimmel, Jessica Becker, Sophia Peters, Hela Hundertmark

Hum Genet· May 2018

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High-power mid-infrared frequency comb source based on a femtosecond Er:fiber oscillator.
Feng Zhu, Holger Hundertmark, Alexandre A Kolomenskii, James Strohaber, Ronald Holzwarth

Opt Lett· July 2013

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