Schraders, M., Lee, K., Oostrik, J., Huygen, P. L., Ali, G., Hoefsloot, L. H., . . . Kremer, H. (2010). Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. Elsevier.
Chicago Style CitationSchraders, Margit, et al. Homozygosity Mapping Reveals Mutations of GRXCR1 As a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. Elsevier, 2010.
Cita MLASchraders, Margit, et al. Homozygosity Mapping Reveals Mutations of GRXCR1 As a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. Elsevier, 2010.
Atenció: Aquestes cites poden no estar 100% correctes.