Related Articles
Developmental delay referrals and the roles of Fragile X testing and molecular karyotyping: A New Zealand perspective
Premature ovarian failure and FMR1 premutation co-segregation in a large Brazilian family
Assessment of efficacy of prenatal genetic diagnosis for fragile X syndrome using nested PCR
The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males
Alternatively spliced products lacking exon 12 dominate the expression of fragile X mental retardation 1 gene in human tissues