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	1.	Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activation. [electronic resource] by Lew, Erin D Bae, Jae Hyun Rohmann, Edyta Wollnik, Bernd Schlessinger, Joseph Producer: 20080111 In: Proceedings of the National Academy of Sciences of the United States of America vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Activating somatic FGFR2 mutations in breast cancer. [electronic resource] by Reintjes, Nadine Li, Yun Becker, Alexandra Rohmann, Edyta Schmutzler, Rita Wollnik, Bernd Producer: 20130917 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway. [electronic resource] by Shams, Imad Rohmann, Edyta Eswarakumar, Veraragavan P Lew, Erin D Yuzawa, Satoru Wollnik, Bernd Schlessinger, Joseph Lax, Irit Producer: 20080122 In: Molecular and cellular biology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Reduction of PCR-amplifiable DNA by ethylene oxide treatment of forensic consumables. [electronic resource] by Neureuther, Katharina Rohmann, Edyta Hilken, Manuela Sonntag, Marie-Luise Herdt, Silke Koennecke, Thomas Jacobs, Roland Adamski, Michalina Reisbacher, Stefan Alfs, Knut Strain, Peter Bastisch, Ingo Producer: 20150402 In: Forensic science international. Genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutations in different components of FGF signaling in LADD syndrome. [electronic resource] by Rohmann, Edyta Brunner, Han G Kayserili, Hülya Uyguner, Oya Nürnberg, Gudrun Lew, Erin D Dobbie, Angus Eswarakumar, Veraragavan P Uzumcu, Abdullah Ulubil-Emeroglu, Melike Leroy, Jules G Li, Yun Becker, Christian Lehnerdt, Kai Cremers, Cor W R J Yüksel-Apak, Memnune Nürnberg, Peter Kubisch, Christian Kubisch, Chriütian Schlessinger, Joseph van Bokhoven, Hans Wollnik, Bernd Producer: 20060614 In: Nature genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. [electronic resource] by Kalay, Ersan Li, Yun Uzumcu, Abdullah Uyguner, Oya Collin, Rob W Caylan, Refik Ulubil-Emiroglu, Melike Kersten, Ferry F J Hafiz, Gunter van Wijk, Erwin Kayserili, Hulya Rohmann, Edyta Wagenstaller, Janine Hoefsloot, Lies H Strom, Tim M Nürnberg, Gudrun Baserer, Nermin den Hollander, Anneke I Cremers, Frans P M Cremers, Cor W R J Becker, Christian Brunner, Han G Nürnberg, Peter Karaguzel, Ahmet Basaran, Seher Kubisch, Christian Kremer, Hannie Wollnik, Bernd Producer: 20060807 In: Human mutation vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)