Cite
HARVARD Citation
Milà, M. et al. (1996). Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.. Journal of medical genetics. 33 (4), pp. 338-340. [Online].
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Milà, M. et al. (1996). Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.. Journal of medical genetics. 33 (4), pp. 338-340. [Online].