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Einrichtung
Medientyp
- Text 4
Karte
Erscheinungsjahr
Autor/in
- Seemanova, Eva
- Abdollahpour, Hengameh 2
- Alawi, Malik 2
- Gillessen-Kaesbach, Gabriele 2
- Kortüm, Fanny 2
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Sprache
4 Einträge gefunden
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An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome
- Abdollahpour, Hengameh
- Alawi, Malik
- Kortüm, Fanny
- Beckstette, Michael
- Seemanova, Eva
- Komárek, Vladimír
- Rosenberger, Georg
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Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
- Harmsen, May-Britt
- Azzarello-Burri, Silvia
- González, García
- Mar, M
- Gillessen-Kaesbach, Gabriele
- Meinecke, Peter
- Müller, Dietmar
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