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Q21183965-90A869AE-4FC2-4C15-ADC0-F21E2DCA992D
Q21183965-90A869AE-4FC2-4C15-ADC0-F21E2DCA992D
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http://www.wikidata.org/entity/statement/Q21183965-90A869AE-4FC2-4C15-ADC0-F21E2DCA992D
Personal genome testing in medical education: student experiences with genotyping in the classroom
P2860
Q21183965-90A869AE-4FC2-4C15-ADC0-F21E2DCA992D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21183965-90A869AE-4FC2-4C15-ADC0-F21E2DCA992D
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e480e76f6cc4aafd0e643fdd0469334da105dd7b
P2860
Report on the p.Ser489X (p.Ser489*) CFTR mutation, a variant with severe associated phenotype and high prevalence in a Quebec French-Canadian cystic fibrosis patient population.