Title |
A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype / Christiane Zweier, Cornelia Kraus, Louise Brueton, Trevor Cole, Franziska Degenhardt, Hartmut Engels, Gabriele Gillessen-Kaesbach, Luitgard Graul-Neumann, Denise Horn, Juliane Hoyer, Walter Just, Anita Rauch, André Reis, Bernd Wollnik, Michael Zeschnigk, Hermann-Josef Lüdecke, Dagmar Wieczorek |
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Involved |
Christiane Zweier (Verfasser)
Cornelia Kraus (Verfasser) Louise Brueton (Verfasser) Trevor Cole (Verfasser)
Franziska Degenhardt (Verfasser)
Hartmut Engels (Verfasser) Gabriele Gillessen-Kaesbach (Verfasser) Luitgard Graul-Neumann (Verfasser) Denise Horn (Verfasser) Juliane Hoyer (Verfasser) Walter Just (Verfasser) Anita Rauch (Verfasser) André Reis (Verfasser) Bernd Wollnik (Verfasser) Michael Zeschnigk (Verfasser) Hermann-Josef Lüdecke (Verfasser) Dagmar Wieczorek (Verfasser) |
Published |
Erlangen: Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) |
Extent |
Online-Ressource |
Language |
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Country |
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Topic |
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Subject |
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DDC notation |
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Persistent identifier |
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Further information |
In: Journal of Medical Genetics 50.12 (2013): S. 838-847. <http://jmg.bmj.com/content/50/12/838> |
Record ID |
1124234128 |
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