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- Text 7
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Autor/in
- Kutsche, Kerstin
- Harms, Frederike L 3
- Alawi, Malik 2
- Nampoothiri, Sheela 2
- Yesodharan, Dhanya 2
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Sprache
- Englisch 7
7 Einträge gefunden
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RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1
- Meyer Zum Büschenfelde, Uta
- Brandenstein, Laura Isabel
- von Elsner, Leonie
- Flato, Kristina
- Holling, Tess
- Zenker, Martin
- Rosenberger, Georg
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Goltz-Gorlin Syndrome: Revisiting the Clinical Spectrum
- Yesodharan, Dhanya
- Büschenfelde, Uta Meyer Zum
- Kutsche, Kerstin
- Mohandas Nair, K
- Nampoothiri, Sheela
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Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder
- Harms, Frederike L
- Kloth, Katja
- Bley, Annette
- Denecke, Jonas
- Santer, René
- Lessel, Davor
- Hempel, Maja
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The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor
- Harms, Frederike L
- Alawi, Malik
- Amor, David J
- Tan, Tiong Y
- Cuturilo, Goran
- Lissewski, Christina
- Brinkmann, Julia
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Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation
2018 - Forschungsinformationssystem des UKE -
Elsahy-Waters syndrome is caused by biallelic mutations in CDH11
- Harms, Frederike L
- Nampoothiri, Sheela
- Anazi, Shams
- Yesodharan, Dhanya
- Alawi, Malik
- Kutsche, Kerstin
- Alkuraya, Fowzan S