Institut für Humangenetik der Uniklinik Aachen
        
    Description of facility
Director / Spokesperson
Prof. Dr. med. Ingo KurthInformation
Care facility for adults and childrenDescription
            Im Rahmen der akkreditierten Diagnostik kommen moderne Methoden wie die Hochdurchsatzsequenzierung am Institut für Humangenetik zum Einsatz. Neben Lehrangeboten für Studierende finden Sie auf der Website Details zu den Forschungsprojekten des Instituts. Es ist ein zentrales Anliegen des Instituts, die molekularen Ursachen genetischer Erkrankungen zu verstehen.
        
    Consultation hours
nach Vereinbarung.
Care provisions
This facility offers the following
- Genetic counselling
- Diagnostic
Contact
            
             Sekretariat
            
             0241 8085572
            
             0241 8082580
            
            
            humangenetik@ukaachen.de
            
            
             Website
        http://www.humangenetik.ukaachen.de/
        
        
Secondary Contact
                
                     Terminvergabe für Sprechstunde
                
                 0241 8085572
                
                
                
            
Languages
            
            
            
            
             Deutsch
 Deutsch
            
             Englisch
 Englisch
            
            
            
    
European Reference Network 1
Preview of the assigned diseases 3
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to CDKN1C mutation
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to 11p15 microdeletion
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion
                        
                    
                        
                        
                        Silver-Russell syndrome due to an imprinting defect of 11p15
                        
                    
                        
                        
                        Silver-Russell syndrome due to 7p11.2p13 microduplication
                        
                    
                        
                        
                        Silver-Russell syndrome due to 11p15 microduplication
                        
                    
                        
                        
                        Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
                        
                    
                        
                        
                        Bardet-Biedl syndrome
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome
                        
                    
                        
                        
                        Silver-Russell syndrome
                        
                    
                        
                        
                        Silver-Russell syndrome due to a point mutation
                        
                    
                        
                        
                        Meckel syndrome
                        
                    
                        
                        
                        Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
                        
                    
                        
                        
                        Autosomal dominant polycystic kidney disease
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to 11p15 microduplication
                        
                    
                        
                        
                        Joubert syndrome
                        
                    
                        
                        
                        Beckwith-Wiedemann syndrome due to NSD1 mutation
                        
                    
                
            6.044572716416757550.7769086Institut für Humangenetik der Uniklinik Aachen
            
        Last updated:
        27.12.2024
    
