The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype.

Grasso, Marina

The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype. [electronic resource] - Molecular and cellular probes Apr 2010 - 107-9 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1096-1194

10.1016/j.mcp.2009.10.006 doi


Aged, 80 and over
Base Sequence
Child
DNA Mutational Analysis
Female
Fragile X Mental Retardation Protein--genetics
Fragile X Syndrome--genetics
Genetic Predisposition to Disease
Humans
Infant, Newborn
Male
Molecular Sequence Data
Pedigree
Phenotype
Polymorphism, Single Nucleotide--genetics
Pregnancy
Promoter Regions, Genetic--genetics