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A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia. [electronic resource] by
- Ramsebner, Reinhard
- Ludwig, Martin
- Parzefall, Thomas
- Lucas, Trevor
- Baumgartner, Wolf-Dieter
- Bodamer, Olaf
- Cengiz, Filiz Basak
- Schoefer, Christian
- Tekin, Mustafa
- Frei, Klemens
Producer: 20100216
In:
The Laryngoscope vol. 120
Availability: No items available.
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Increased FGF3 and FGF4 gene dosage is a risk factor for craniosynostosis. [electronic resource] by
- Grillo, Lucia
- Greco, Donatella
- Pettinato, Rosa
- Avola, Emanuela
- Potenza, Nabor
- Castiglia, Lucia
- Spalletta, Angela
- Amata, Silvestra
- Di Benedetto, Daniela
- Luciano, Daniela
- Romano, Corrado
- Fichera, Marco
Producer: 20140417
In:
Gene vol. 534
Availability: No items available.
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