Sensenbrenner syndrome (Cranioectodermal dysplasie): Clinical and molecular analysis of 39 patients including two new patients

Publication year

2013

Author(s)

Keppler-Noreuil, K.

Source

American Journal of Medical Genetics. Part A, 161, 11, (2013), pp. 2762-76

ISSN

DOI

https://doi.org/10.1002/ajmg.a.36265

Publication type

Article / Letter to editor

Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/125895

https://hdl.handle.net/2066/125895

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