Familial colorectal cancer Type X
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Genetic Advices 2
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
Schwabachanlage 10
91054 Erlangen
09131 8522318
09131 8523232
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- Constitutional mismatch repair deficiency syndrome
- Li-Fraumeni syndrome
- Xeroderma pigmentosum
- Noonan syndrome
- Full NF2-related schwannomatosis
- Diamond-Blackfan anemia
- Von Hippel-Lindau disease
- Familial ovarian cancer
- Inherited cancer-predisposing syndrome
- Silver-Russell syndrome
- Ataxia-telangiectasia
- Hereditary retinoblastoma
- Common variable immunodeficiency
- Beckwith-Wiedemann syndrome
- Hereditary nonpolyposis colon cancer
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
Martinistraße 52
20251 Hamburg
040 741053125
040 741055138
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- Costello syndrome
- Ataxia-telangiectasia
- Familial ovarian cancer
- Full NF2-related schwannomatosis
- APC-related attenuated familial adenomatous polyposis
- Cockayne syndrome
- Silver-Russell syndrome
- Xeroderma pigmentosum
- Inherited renal cancer-predisposing syndrome
- Beckwith-Wiedemann syndrome
- Maffucci syndrome
- Diamond-Blackfan anemia
- Li-Fraumeni syndrome
- Von Hippel-Lindau disease
- Noonan syndrome