Biondi, Maria L., Marasini, Bianca, Leviti, Simona, Turri, Olivia, Bernini, Mara, Seminati, Raffaella, Porreca, Wanda and Guagnellini, Emma. "Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients"
, vol. 39, no. 3, 2001, pp. 281-282.
https://doi.org/10.1515/CCLM.2001.043Biondi, M., Marasini, B., Leviti, S., Turri, O., Bernini, M., Seminati, R., Porreca, W. & Guagnellini, E. (2001). Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients.
,
39(3), 281-282.
https://doi.org/10.1515/CCLM.2001.043Biondi, M., Marasini, B., Leviti, S., Turri, O., Bernini, M., Seminati, R., Porreca, W. and Guagnellini, E. (2001) Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients. Vol. 39 (Issue 3), pp. 281-282.
https://doi.org/10.1515/CCLM.2001.043Biondi, Maria L., Marasini, Bianca, Leviti, Simona, Turri, Olivia, Bernini, Mara, Seminati, Raffaella, Porreca, Wanda and Guagnellini, Emma. "Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients"
39, no. 3 (2001): 281-282.
https://doi.org/10.1515/CCLM.2001.043Biondi M, Marasini B, Leviti S, Turri O, Bernini M, Seminati R, Porreca W, Guagnellini E. Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients. 2001;39(3): 281-282.
https://doi.org/10.1515/CCLM.2001.043Copied to clipboard
