APA

van Riel E., Ausems M. G., Hogervorst F. B., Kluijt I., van Gijn M. E., van Echtelt J., Scheidel-Jacobse K., Hennekam E. F., Stulp R. P., Vos Y. J., Offerhaus G. J. A., Menko F. H. & Gille J. J. (20110714). A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. : Hereditary cancer in clinical practice.

Chicago

van Riel Els, Ausems Margreet Gem, Hogervorst Frans Bl, Kluijt Irma, van Gijn Marielle E, van Echtelt Jeanne, Scheidel-Jacobse Karen, Hennekam Eric Fam, Stulp Rein P, Vos Yvonne J, Offerhaus G Johan A, Menko Fred H and Gille Johan Jp. 20110714. A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. : Hereditary cancer in clinical practice.

Harvard

van Riel E., Ausems M. G., Hogervorst F. B., Kluijt I., van Gijn M. E., van Echtelt J., Scheidel-Jacobse K., Hennekam E. F., Stulp R. P., Vos Y. J., Offerhaus G. J. A., Menko F. H. and Gille J. J. (20110714). A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. : Hereditary cancer in clinical practice.

MLA

van Riel Els, Ausems Margreet Gem, Hogervorst Frans Bl, Kluijt Irma, van Gijn Marielle E, van Echtelt Jeanne, Scheidel-Jacobse Karen, Hennekam Eric Fam, Stulp Rein P, Vos Yvonne J, Offerhaus G Johan A, Menko Fred H and Gille Johan Jp. A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. : Hereditary cancer in clinical practice. 20110714.