Matches in Nanopublications for { ?s ?p "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP258.RAkXjOR4CcgZ2EAi4yXeRr8AtdIn5yrR_Z85ddZQCOUaY130_assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258.RAkXjOR4CcgZ2EAi4yXeRr8AtdIn5yrR_Z85ddZQCOUaY130_provenance.
- assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- NP343.RADnNDP2EX0eo-5bnpFPI_myKrtfKlvXFITRfJgCWzkaE130_assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343.RADnNDP2EX0eo-5bnpFPI_myKrtfKlvXFITRfJgCWzkaE130_provenance.
- NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.