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| Oncology |
| Multiple endocrine Neoplasia Type 1 (MEN 1-Gene, MIM 131100) |
| Multiple endocrine Neoplasia Type 2 (RET-Protooncogene, MIM 171400) |
| Multiple Pheochromocytoma, Paraganglioma (Succinat Dehydrogenase Subunit D, SDHD-Gene, MIM 602690; Succinat Dehydrogenase Subunit B, SDHB-Gene, MIM 185470) |
| Hereditäry non-polyposis Colon-Carcinoma, HNPCC (Mikrosatelliten-Instabilität) |
| Li Fraumeni-Syndrom (Tumorsuppressor-Gene p53, TP53, MIM191170) |
| Peutz-Jeghers Syndrome (Hamatomas intestinal polyposis, Serin/Threonin Proteinkinase 11-Gene, PJS, MIM602216) |
| Neurofibromatose Type 1 (Neurofibromin-Gene, NF1, MIM 162200) |
| HPT-Jaw Tumor Syndrome (HRTP2, Parafibromin-Gen, MIM 145001) |
| Von Hippel-Lindau-Syndrome (VHL-Gen, MIM 193300) |
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