APA

Aquaron R., Soufir N., Bergé-Lefranc J., Badens C., Austerlitz F. & Grandchamp B. (20071109). Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene. : Journal of human genetics.

Chicago

Aquaron Robert, Soufir Nadem, Bergé-Lefranc Jean-Louis, Badens Catherine, Austerlitz Frederic and Grandchamp Bernard. 20071109. Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene. : Journal of human genetics.

Harvard

Aquaron R., Soufir N., Bergé-Lefranc J., Badens C., Austerlitz F. and Grandchamp B. (20071109). Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene. : Journal of human genetics.

MLA

Aquaron Robert, Soufir Nadem, Bergé-Lefranc Jean-Louis, Badens Catherine, Austerlitz Frederic and Grandchamp Bernard. Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene. : Journal of human genetics. 20071109.