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

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Bibliographic Details
Main Authors:	Kouz, Karim (Author) , Lißewski, Christina (Author) , Spranger, Stephanie (Author) , Mitter, Diana (Author) , Riess, Angelika (Author) , Lopez-Gonzalez, Vanesa (Author) , Lüttgen, Sabine (Author) , Aydin, Hatip (Author) , Deimling, Florian von (Author) , Evers, Christina (Author) , Hahn, Andreas (Author) , Hempel, Maja (Author) , Issa, Ulrike (Author) , Kahlert, Anne-Karin (Author) , Lieb, Adrian (Author) , Villavicencio Lorini, Pablo (Author) , Ballesta-Martinez, Maria Juliana (Author) , Nampoothiri, Sheela (Author) , Ovens-Raeder, Angela (Author) , Puchmajerová, Alena (Author) , Satanovskij, Robin (Author) , Seidel, Heide (Author) , Unkelbach, Stephan (Author) , Zabel, Bernhard (Author) , Kutsche, Kerstin (Author) , Zenker, Martin (Author)
Format:	Article (Journal)
Language:	English
Published:	2016
In:	Genetics in medicine Year: 2016, Volume: 18, Issue: 12, Pages: 1226-1234
ISSN:	1530-0366
DOI:	10.1038/gim.2016.32
Online Access:	Resolving-System, Volltext: http://dx.doi.org/10.1038/gim.2016.32
Author Notes:	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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Physical Description:	Online Resource
ISSN:	1530-0366
DOI:	10.1038/gim.2016.32