APA

Medlej-Hashim M., Mustapha M., Chouery E., Weil D., Parronaud J., Salem N., Delague V., Loiselet J., Lathrop M., Petit C. & Mégarbané A. (20030221). Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. : European journal of human genetics : EJHG.

Chicago

Medlej-Hashim Myrna, Mustapha Mirna, Chouery Eliane, Weil Dominique, Parronaud Joel, Salem Nabiha, Delague Valérie, Loiselet Jacques, Lathrop Mark, Petit Christine and Mégarbané André. 20030221. Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. : European journal of human genetics : EJHG.

Harvard

Medlej-Hashim M., Mustapha M., Chouery E., Weil D., Parronaud J., Salem N., Delague V., Loiselet J., Lathrop M., Petit C. and Mégarbané A. (20030221). Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. : European journal of human genetics : EJHG.

MLA

Medlej-Hashim Myrna, Mustapha Mirna, Chouery Eliane, Weil Dominique, Parronaud Joel, Salem Nabiha, Delague Valérie, Loiselet Jacques, Lathrop Mark, Petit Christine and Mégarbané André. Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. : European journal of human genetics : EJHG. 20030221.