Bolze, A., Boisson, B., Bosch, B., Antipenko, A., Bouaziz, M., Sackstein, P., . . . Casanova, J. (2018). Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons. National Academy of Sciences.
Chicago Style (17. basım) AtıfBolze, A., et al. Incomplete Penetrance for Isolated Congenital Asplenia in Humans with Mutations in Translated and Untranslated RPSA Exons. National Academy of Sciences, 2018.
MLA (9th ed.) AtıfBolze, A., et al. Incomplete Penetrance for Isolated Congenital Asplenia in Humans with Mutations in Translated and Untranslated RPSA Exons. National Academy of Sciences, 2018.
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