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Showing posts with label
Cohesinopathy
.
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Showing posts with label
Cohesinopathy
.
Show all posts
Friday, 15 May 2020
Cohesinopathies, including Cornelia de Lange syndrome and the overlapping phenotype SMC3, causing altered gene expression
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Today’s post is in response to a request from a parent interested in a very rare genetic condition involving the SMC3 ( Structural Maint...
15 comments:
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