Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP49874.RAYEvEKyhJQkhAunLjuAn1H_6-jLl9WpzP0Ww4GGJii7k130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49874.RAYEvEKyhJQkhAunLjuAn1H_6-jLl9WpzP0Ww4GGJii7k130_provenance.
• NP92594.RATLtOuO8aib4TU0JO87Oy4YNDfAeXR_s3p32fj3Ej-WI130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92594.RATLtOuO8aib4TU0JO87Oy4YNDfAeXR_s3p32fj3Ej-WI130_provenance.
• NP89978.RAuu1o3UVhQC96sIyzpO4ll6APrIMwcIzdDTbg9lj_msE130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89978.RAuu1o3UVhQC96sIyzpO4ll6APrIMwcIzdDTbg9lj_msE130_provenance.
• NP82897.RA7ZDcrtRxGaTLGLgzR4b8TrvK-gu42kA-RlJp_kEBuLc130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82897.RA7ZDcrtRxGaTLGLgzR4b8TrvK-gu42kA-RlJp_kEBuLc130_provenance.
• NP89164.RA1oDwvmPeXNR0e5_TNCxZUqfw6RwbAqpQEG1ptib4vVc130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89164.RA1oDwvmPeXNR0e5_TNCxZUqfw6RwbAqpQEG1ptib4vVc130_provenance.
• NP89415.RA0cMUBJfPa_arDV8q3ApgSB0iEpGuL2sxaYzqE-rcRe4130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89415.RA0cMUBJfPa_arDV8q3ApgSB0iEpGuL2sxaYzqE-rcRe4130_provenance.
• NP91615.RA53XtdZq3rihkozGo_TdlaHOtgKqLy60rAeHXtfY_LMo130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91615.RA53XtdZq3rihkozGo_TdlaHOtgKqLy60rAeHXtfY_LMo130_provenance.
• NP52243.RAXVfJS1bLt9EQVqINfozWmwfKxW2pCmncD_mFtrawnw0130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52243.RAXVfJS1bLt9EQVqINfozWmwfKxW2pCmncD_mFtrawnw0130_provenance.
• NP53261.RAeMR8nxIih2h3ufGEkBGJhUnGJ1kCYI2qhic-8eozR2w130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53261.RAeMR8nxIih2h3ufGEkBGJhUnGJ1kCYI2qhic-8eozR2w130_provenance.
• NP84171.RAWJpQel7rZaz-7gVm1x8i3drBXcfpL1qiQnoHCRE7IIg130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84171.RAWJpQel7rZaz-7gVm1x8i3drBXcfpL1qiQnoHCRE7IIg130_provenance.
• NP84552.RAR3rfgxu7O97agmGQFtdbi4o2tnI12Mb6BK8PqTv0-xk130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84552.RAR3rfgxu7O97agmGQFtdbi4o2tnI12Mb6BK8PqTv0-xk130_provenance.
• NP91533.RAUVSh7CsUHd9-1t_tG4QisYOiL5kUpTM34HWKdZ3ODTE130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91533.RAUVSh7CsUHd9-1t_tG4QisYOiL5kUpTM34HWKdZ3ODTE130_provenance.
• NP68443.RAmyv2q5sEJI6ltme_Beet1fOin3ZtoAU0Iq64m7HTuTk130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68443.RAmyv2q5sEJI6ltme_Beet1fOin3ZtoAU0Iq64m7HTuTk130_provenance.
• NP52201.RAFb5gkzZ31qfFixoPoSz52hTKXPmsjeqrmEZP6DcL0Jo130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52201.RAFb5gkzZ31qfFixoPoSz52hTKXPmsjeqrmEZP6DcL0Jo130_provenance.
• NP52203.RAE356FIE1xZ6x4pe7x6kNzkw2INVYrgeQl31JgWs_KEE130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52203.RAE356FIE1xZ6x4pe7x6kNzkw2INVYrgeQl31JgWs_KEE130_provenance.
• NP68808.RAM_wrYBR_4GEh6kgKulEONZF_Zu17A0GfMH_MAtNUoqE130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68808.RAM_wrYBR_4GEh6kgKulEONZF_Zu17A0GfMH_MAtNUoqE130_provenance.
• NP92636.RAjna4IxahAk0xl-_0BUC8yV9QzLMw5PI9Kra7fdGxnrk130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92636.RAjna4IxahAk0xl-_0BUC8yV9QzLMw5PI9Kra7fdGxnrk130_provenance.
• NP89231.RAN4BapCMCb3lcxMmy_knfZ9P-QgkUzl04yRShlrIrJXQ130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89231.RAN4BapCMCb3lcxMmy_knfZ9P-QgkUzl04yRShlrIrJXQ130_provenance.
• NP89455.RAG5DxoTqT67fNtxgsuLQdL-0WcQjUwmH83gNRfyn__R0130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89455.RAG5DxoTqT67fNtxgsuLQdL-0WcQjUwmH83gNRfyn__R0130_provenance.