Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation

od Kruis, Tassilo, Klammt, Jürgen, Galli-Tsinopoulou, Assimina, Wallborn, Tillmann, Schlicke, Marina, Müller, Eva, Kratzsch, Jürgen, Körner, Antje, Odeh, Rasha, Kiess, Wieland, Pfäffle, Roland
Izdano u Mol Endocrinol (2010)

Genetic analyses of bone morphogenetic protein 2, 4 and 7 in congenital combined pituitary hormone deficiency

od Breitfeld, Jana, Martens, Susanne, Klammt, Jürgen, Schlicke, Marina, Pfäffle, Roland, Krause, Kerstin, Weidle, Kerstin, Schleinitz, Dorit, Stumvoll, Michael, Führer, Dagmar, Kovacs, Peter, Tönjes, Anke
Izdano 2013

A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal...

od Wallborn, Tillmann, Wüller, Stefan, Klammt, Jürgen, Kruis, Tassilo, Kratzsch, Jürgen, Schmidt, Gabriele, Schlicke, Marina, Müller, Eva, Schmitz van de Leur, Hildegard, Kiess, Wieland, Pfäffle, Roland
Izdano u Mol Endocrinol (2010)

IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)

od Janchevska, Aleksandra, Krstevska-Konstantinova, Marina, Pfäffle, Heike, Schlicke, Marina, Laban, Nevenka, Tasic, Velibor, Gucev, Zoran, Mironska, Kristina, Dimovski, Aleksandar, Kratzsch, Jürgen, Klammt, Jürgen, Pfäffle, Roland
Izdano u Open Access Maced J Med Sci (2018)

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

od Bertko, Eleonore, Klammt, Jürgen, Dusatkova, Petra, Bahceci, Mithat, Gonc, Nazli, ten Have, Louise, Kandemir, Nurgun, Mansmann, Georg, Obermannova, Barbora, Oostdijk, Wilma, Pfäffle, Heike, Rockstroh-Lippold, Denise, Schlicke, Marina, Tuzcu, Alpaslan Kemal, Pfäffle, Roland
Izdano u J Hum Genet (2017)