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5 Treffer

Kurzansicht	E-Jahr	Zugriff	Typ	Operations
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder 2021 . Dworschak, Gabriel \| Reutter, Heiko M. \| Ludwig, Michael	2021		http://purl.org/ontology/bibo/Article
Dysregulated paired related homeobox 1 impacts on hepatocellular carcinoma phenotypes 2021 . Piorońska, Weronika \| Nwosu, Zeribe Chike \| Han, Mei \| Büttner, Michael \| Ebert, Matthias Philip \| Dooley, Steven \| Meyer, Christoph	2021		http://purl.org/ontology/bibo/Article
Converting fibroblastic fates leads to wound healing without scar 2021 . Jiang, Dongsheng \| Rinkevich, Yuval	2021		http://purl.org/ontology/bibo/Article
Genome sequencing in families with congenital limb malformations 2021 . Elsner, Jonas \| Mensah, Martin A. \| Holtgrewe, Manuel \| Hertzberg, Jakob \| Bigoni, Stefania \| Busche, Andreas \| Coutelier, Marie \| de Silva, Deepthi C. \| Elçioglu, Nursel \| Filges, Isabel \| Gerkes, Erica \| Girisha, Katta M. \| Graul-Neumann, Luitgard \| Jamsheer, Aleksander \| Krawitz, Peter \| Kurth, Ingo \| Markus, Susanne \| Megarbane, Andre \| Reis, André \| Reuter, Miriam S. \| Svoboda, Daniel \| Teller, Christopher \| Tuysuz, Beyhan \| Türkmen, Seval \| Wilson, Meredith \| Woitschach, Rixa \| Vater, Inga \| Caliebe, Almuth \| Hülsemann, Wiebke \| Horn, Denise \| Mundlos, Stefan \| Spielmann, Malte	2021		http://purl.org/ontology/bibo/Article
Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update 2021 . Schätzl, Teresa \| Kaiser, Lars \| Deigner, Hans-Peter	2021		http://purl.org/ontology/bibo/Article