Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
by 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)
,
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