Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2016
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| In: |
Genetics in medicine
Year: 2016, Jahrgang: 18, Heft: 12, Pages: 1226-1234 |
| ISSN: | 1530-0366 |
| DOI: | 10.1038/gim.2016.32 |
| Online-Zugang: | Resolving-System, Volltext: http://dx.doi.org/10.1038/gim.2016.32
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| Verfasserangaben: | Karim Kouz, Christina Lissewski, Stephanie Spranger, MD, Diana Mitter, MD, Angelika Riess, MD, Vanesa Lopez-Gonzalez, MD, Sabine Lüttgen, MD, Hatip Aydin, MD, Florian von Deimling, MD, Christina Evers, MD, Andreas Hahn, MD, Maja Hempel, MD, Ulrike Issa, MD, Anne-Karin Kahlert, MD, Adrian Lieb, MD, Pablo Villavicencio-Lorini, MD, Maria Juliana Ballesta-Martinez, MD, Sheela Nampoothiri, MD, Angela Ovens-Raeder, MD, Alena Puchmajerová, MD, Robin Satanovskij, MD, Heide Seidel, MD, Stephan Unkelbach, MD, Bernhard Zabel, MD, Kerstin Kutsche, PhD and Martin Zenker, MD |
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