Genetic modifiers in rare disorders: the case of fragile X syndrome (2020)
Attributed to:
Integrating innovative technologies for genotyping and phenotyping in stratified medicine
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-020-00711-x
PubMed Identifier: 32862204
Publication URI: http://europepmc.org/abstract/MED/32862204
Type: Journal Article/Review
Parent Publication: European Journal of Human Genetics
Issue: 1
ISSN: 1018-4813