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Journal Article

Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome)

MPS-Authors
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Ropers,  H.-H.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Tzschach,  A.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Institute of Human Genetics, University of Tübingen;

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Hoffer.pdf
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Citation

Hoffer, J. L., Fryssira, H., Konstantinidou, A., Ropers, H.-H., & Tzschach, A. (2013). Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical Genetics: an international journal of genetics in medicine, 83(1), 92-95. doi:10.1111/j.1399-0004.2012.01880.x.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-EC6E-9
Abstract
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