Search Results - López-González, Vanesa

PHIP-associated Chung-Jansen syndrome: report of 23 new individuals by Kampmeier, Antje (Author) , Leitão, Elsa (Author) , Parenti, Ilaria (Author) , Beygo, Jasmin (Author) , Depienne, Christel (Author) , Bramswig, Nuria C (Author) , Hsieh, Tzung-Chien (Author) , Afenjar, Alexandra (Author) , Beck-Wödl, Stefanie (Author) , Grasshoff, Ute (Author) , Haack, Tobias B (Author) , Bijlsma, Emilia K (Author) , Ruivenkamp, Claudia (Author) , Lausberg, Eva (Author) , Elbracht, Miriam (Author) , Haanpää, Maria K (Author) , Koillinen, Hannele (Author) , Heinrich, Uwe (Author) , Rost, Imma (Author) , Jamra, Rami Abou (Author) , Popp, Denny (Author) , Koch-Hogrebe, Margarete (Author) , Rostasy, Kevin (Author) , López-González, Vanesa (Author) , Sanchez-Soler, María José (Author) , Macedo, Catarina (Author) , Schmetz, Ariane (Author) , Steinborn, Carmen (Author) , Weidensee, Sabine (Author) , Lesmann, Hellen (Author) , Marbach, Felix (Author) , Caro, Pilar (Author) , Schaaf, Christian P. (Author) , Krawitz, Peter (Author) , Wieczorek, Dagmar (Author) , Kaiser, Frank J (Author) , Kuechler, Alma (Author) ,

• Verlag, lizenzpflichtig, Volltext

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) ,

• Resolving-System, Volltext

Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension by Pfarr, Nicole (Author) , Fischer, Christine (Author) , Benjamin, Nicola (Author) , Becker-Grünig, Tabea (Author) , López-González, Vanesa (Author) , Gorenflo, Matthias (Author) , Hager, Alfred (Author) , Hinderhofer, Katrin (Author) , Miera, Oliver (Author) , Nagel, Christian (Author) , Schranz, Dietmar (Author) , Grünig, Ekkehard (Author) ,

• Verlag, lizenzpflichtig, Volltext