Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.

Milà, M

Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation. [electronic resource] - Human genetics Oct 1997 - 503-7 p. digital

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

0340-6717

10.1007/s004390050542 doi


Adolescent
Adult
Child
Child, Preschool
Chromosome Fragile Sites
Chromosome Fragility
DNA Methylation
Female
Fragile X Mental Retardation Protein
Fragile X Syndrome--genetics
Genetic Testing
Humans
Male
Mosaicism
Mutation--genetics
Nerve Tissue Proteins--genetics
Nuclear Proteins
Phenotype
Proteins--genetics
Psychotic Disorders--genetics
RNA-Binding Proteins
Schools
Spain
Trans-Activators
Trinucleotide Repeats--genetics
X Chromosome--genetics