Wang, H., Wang, X., He, C., Li, H., Qing, J., Grati, M., . . . Feng, Y. (2015). Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family. J Hum Genet.
Styl ChicagoWang, Honghan, et al. "Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated With Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family." J Hum Genet 2015.
Citace podle MLAWang, Honghan, et al. "Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated With Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family." J Hum Genet 2015.
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