The authors were able to correct mutations in several well - characterized genetic disorders, including: Duchenne Muscular Dystrophy, Achondroplasia, and MECP2 -
duplication syndrome using cells derived from human patients.
I have spent many years studying 2q23.1 deletion and
duplication syndrome through genotype - phenotype, neural progenitor stem cells, and RNA - seq studies.
Not exact matches
I see
duplication of effort, with denominations and individual churches not working together; and the «not - invented - here»
syndrome, as very often the information or the thing we are trying to produce is already being produced somewhere else.
The shiny object
syndrome will wear off and users of technology will truly care about the location, access and
duplication of their data.