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OHSU 13 records found 1 - 10nextSearch took 0.19 seconds. 
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Despite their devastating impacts on millions of people, most rare and congenital disorders remain poorly understood, leaving the patients with these disorders with no FD [...]
2023-07-20 | Abstract |
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Individuals who inherit a pathogenic mutation in SDHA have an increased risk of cancer. However, there is often insufficient evidence to properly assess pathogenicity, an [...]
2023-12-14 | Dissertation |
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Neurofibromatosis type 1 (NF1) is a genetically determined neurodevelopmental disorder and tumor syndrome with an incidence of approximately 1/3000 live births. A progre [...]
2020 | Abstract |

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