Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutations.

MLA

Filippi, G., et al. “Premutation for the Martin-Bell Syndrome Analyzed in a Large Pedigree Segregating Also for G6PD-Deficiency. I: A Working Hypothesis on the Nature of the FRAX-Mutations.” American Journal of Medical Genetics, vol. 40, no. 4, Sept. 1991, pp. 387–94. EBSCOhost, https://doi.org/10.1002/ajmg.1320400402.

APA

Filippi, G., Arslanian, A., Dagna-Bricarelli, F., Pierluigi, M., Grasso, M., Rinaldi, A., Rocchi, M., & Siniscalco, M. (1991). Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutations. American Journal of Medical Genetics, 40(4), 387–394. https://doi.org/10.1002/ajmg.1320400402

Chicago

Filippi, G, A Arslanian, F Dagna-Bricarelli, M Pierluigi, M Grasso, A Rinaldi, M Rocchi, and M Siniscalco. 1991. “Premutation for the Martin-Bell Syndrome Analyzed in a Large Pedigree Segregating Also for G6PD-Deficiency. I: A Working Hypothesis on the Nature of the FRAX-Mutations.” American Journal of Medical Genetics 40 (4): 387–94. doi:10.1002/ajmg.1320400402.