Francey, L. J., Conlin, L. K., Kadesch, H. E., Clark, D., Berrodin, D., Sun, Y., . . . Krantz, I. D. (2011). Genome-wide SNP Genotyping Identifies the Stereocilin (STRC) Gene as a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment.
Chicago ZitierstilFrancey, Lauren J., et al. Genome-wide SNP Genotyping Identifies the Stereocilin (STRC) Gene As a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment. 2011.
MLA ZitierstilFrancey, Lauren J., et al. Genome-wide SNP Genotyping Identifies the Stereocilin (STRC) Gene As a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment. 2011.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.