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

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

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

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

由 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
發表在 Mol Endocrinol (2010)

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

由 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
發表在 Open Access Maced J Med Sci (2018)

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

由 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
發表在 J Hum Genet (2017)