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BI, WEIMIN
One or more keywords matched the following items that are connected to
BI, WEIMIN
Item Type
Name
Academic Article
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.
Academic Article
RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome.
Concept
Point Mutation
Academic Article
Whole exome sequencing identifies the first STRADA point mutation in a patient with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE).
Search Criteria
Point Mutation