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Untitled work

Abbeduto (2004) · doi:10.1352/0895-8017(2004)109

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Rousseau, F., Rouillard, P., Morel, M. L., Khandjian, E. W., & Morgan, K. (1995) · Europe PMC (PubMed Central) · Cited by 361

Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother–newborn pairs from the general population

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Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions

Yrigollen, C. M., Mendoza‐Morales, G., Hagerman, R. J., & Tassone, F. (2013) · Journal of Human Genetics · doi:10.1038/jhg.2013.50 · Cited by 11

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome

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Structure and stability upon maternal transmission of common and intermediate FMR1 (Fragile X Mental Retardation 1) alleles in a sample of the Brazilian population

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