APA

Mangino M., Flex E., Capon F., Sangiuolo F., Carraro E., Gualandi F., Mazzoli M., Martini A., Novelli G. & Dallapiccola B. (20011204). Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. : European journal of human genetics : EJHG.

Chicago

Mangino M, Flex E, Capon F, Sangiuolo F, Carraro E, Gualandi F, Mazzoli M, Martini A, Novelli G and Dallapiccola B. 20011204. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. : European journal of human genetics : EJHG.

Harvard

Mangino M., Flex E., Capon F., Sangiuolo F., Carraro E., Gualandi F., Mazzoli M., Martini A., Novelli G. and Dallapiccola B. (20011204). Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. : European journal of human genetics : EJHG.

MLA

Mangino M, Flex E, Capon F, Sangiuolo F, Carraro E, Gualandi F, Mazzoli M, Martini A, Novelli G and Dallapiccola B. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. : European journal of human genetics : EJHG. 20011204.