APA

Brakensiek K., Frye-Boukhriss H., Mälzer M., Abramowicz M., Bahr M. J., von Beckerath N., Bergmann C., Caselitz M., Holinski-Feder E., Muschke P., Oexle K., Strobl-Wildemann G., Wolff G., El-Harith E. A. & Stuhrmann M. (20081111). Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia. : Clinical genetics.

Chicago

Brakensiek K, Frye-Boukhriss H, Mälzer M, Abramowicz M, Bahr M J, von Beckerath N, Bergmann C, Caselitz M, Holinski-Feder E, Muschke P, Oexle K, Strobl-Wildemann G, Wolff G, El-Harith E A and Stuhrmann M. 20081111. Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia. : Clinical genetics.

Harvard

Brakensiek K., Frye-Boukhriss H., Mälzer M., Abramowicz M., Bahr M. J., von Beckerath N., Bergmann C., Caselitz M., Holinski-Feder E., Muschke P., Oexle K., Strobl-Wildemann G., Wolff G., El-Harith E. A. and Stuhrmann M. (20081111). Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia. : Clinical genetics.

MLA

Brakensiek K, Frye-Boukhriss H, Mälzer M, Abramowicz M, Bahr M J, von Beckerath N, Bergmann C, Caselitz M, Holinski-Feder E, Muschke P, Oexle K, Strobl-Wildemann G, Wolff G, El-Harith E A and Stuhrmann M. Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia. : Clinical genetics. 20081111.