Lenassi, E., Vincent, A., Li, Z., Saihan, Z., Coffey, A. J., Steele-Stallard, H. B., . . . Webster, A. R. (2015). A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants. Eur J Hum Genet.
Styl ChicagoLenassi, Eva, et al. "A Detailed Clinical and Molecular Survey of Subjects With Nonsyndromic USH2A Retinopathy Reveals an Allelic Hierarchy of Disease-causing Variants." Eur J Hum Genet 2015.
Citace podle MLALenassi, Eva, et al. "A Detailed Clinical and Molecular Survey of Subjects With Nonsyndromic USH2A Retinopathy Reveals an Allelic Hierarchy of Disease-causing Variants." Eur J Hum Genet 2015.
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