Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation

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Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation

Author: Kouz, Karim; Lissewski, Christina; Spranger, Stephanie; Mitter, Diana; Riess, Angelika; Lopez-Gonzalez, Vanesa; Luettgen, Sabine; Aydin, Hatip; von Deimling, Florian; Evers, Christina; Hahn, Andreas; Hempel, Maja; Issa, Ulrike; Kahlert, Anne-Karin; Lieb, Adrian; Villavicencio-Lorini, Pablo; Juliana Ballesta-Martinez, Maria; Nampoothiri, Sheela; Ovens-Raeder, Angela; Puchmajerova, Alena; Satanovskij, Robin; Seidel, Heide; Unkelbach, Stephan; Zabel, Bernhard; Kutsche, Kerstin; Zenker, Martin
Tübinger Autor(en):
Rieß, Angelika
Published in: Genetics in Medicine (2016), Bd. 18, H. 12, S. 1226-1234
Verlagsangabe: Nature Publishing Group
Language: English
Full text: http://dx.doi.org/10.1038/gim.2016.32
ISSN: 1530-0366
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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