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OHSU 3 records found Search took 0.18 seconds. 
1.
Marfan Syndrome is a genetic condition defined by autosomal dominant variations in the FBN1 gene resulting in changes to the cardiovascular, ocular, and skeletal systems. [...]
2024 | Abstract |
2.
ca. 1958
1958 | Still image | Historical Collections and Archives |
3.
Medical Museum Collection, Box 57
1958 | Still image | Historical Collections and Archives |

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