The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype. [electronic resource]
Producer: 20100719Description: 107-9 p. digitalISSN:- 1096-1194
- 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
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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