Accepted
at 7:24 p.m. Mar, 11, 2024
by
thomas.holmes
Author:
majoratfo
Type of change:
Other
Rationale for change
Reworded for clarity. Before, it could have been misinterpreted that the cloze was asking for the type of mutation (e.g. gain of function, loss of function, etc.). This rewording should make it clear the cloze is asking for the gene name.
Before
After
Text
Text
Text
Text
Extra
MarFan syndrome : FBN1 (codes for fibrillin-1) mutation on chromosome 15 (Fifteen)


Lecture Notes
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Missed Questions
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Pathoma
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Boards and Beyond
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First Aid


Sketchy
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Sketchy 2
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Sketchy Extra
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Picmonic
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Pixorize


Review Marfan Syndrome


Review Marfan Syndrome
Physeo
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Bootcamp
Watch associated Bootcamp video - Aortic Disease: Cardiac Considerations of Marfan Syndrome
Watch associated Bootcamp video - Connective Tissue: Marfan Syndrome
Watch associated Bootcamp video - Connective Tissue: Marfan Syndrome
OME
Additional Resources
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One by one
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