M. Morel

FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome.

A. Reiss, W. Kaufmann, M. Abrams, 1999, American journal of medical genetics.

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

S. Lévesque, F. Rousseau, K. Morgan, 2009, Clinical genetics.

DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature.

F. Rousseau, P. Chiurazzi, M. Pomponi, 1999, American journal of medical genetics.

Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.

S. Lévesque, F. Rousseau, K. Morgan, 2002, Human molecular genetics.

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

É. Khandjian, F. Rousseau, K. Morgan, 1995, American journal of human genetics.