APA

Jonard L., Couloigner V., Pierrot S., Louha M., Gherbi S., Denoyelle F. & Marlin S. (20120605). Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype. : European journal of medical genetics.

Chicago

Jonard Laurence, Couloigner Vincent, Pierrot Sébastien, Louha Malek, Gherbi Souad, Denoyelle Françoise and Marlin Sandrine. 20120605. Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype. : European journal of medical genetics.

Harvard

Jonard L., Couloigner V., Pierrot S., Louha M., Gherbi S., Denoyelle F. and Marlin S. (20120605). Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype. : European journal of medical genetics.

MLA

Jonard Laurence, Couloigner Vincent, Pierrot Sébastien, Louha Malek, Gherbi Souad, Denoyelle Françoise and Marlin Sandrine. Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype. : European journal of medical genetics. 20120605.