Facetten
Zugriff
Einrichtung
Medientyp
- Text 2
Karte
Erscheinungsjahr
Autor/in
- Keyser, Britta
- von Kodolitsch, Yskert
- Arndt, Florian 1
- Arslan-Kirchner, Mine 1
- Binner, Priska 1
- alle zeigen
Sprache
- Englisch 2
2 Einträge gefunden
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Clinical and genetic diagnosis of Marfan syndrome in childhood are Equal- FBN1 mutation should not influence handling of pediatric patients with confirmed Marfansyndrome
- Stark, Veronika
- Arndt, Florian
- Harring, Gesa
- Keyser, Britta
- von Kodolitsch, Yskert
- Kozlik-Feldmann, Rainer
- Kutsche, Kerstin
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High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections
- Kathiravel, Ushanthine
- Keyser, Britta
- Hoffjan, Sabine
- Kötting, Judith
- Müller, Melanie
- Sivalingam, Sugirthan
- Bonin, Michael