Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
• NP625939.RASsGK5fUYoDsdR05xgxNhJ_WoTEYhhzfGQXozKmPO_No130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625939.RASsGK5fUYoDsdR05xgxNhJ_WoTEYhhzfGQXozKmPO_No130_provenance.
• NP261557.RAJUwBs4HfghWZjD8PI2I5GEK8mbLnQFO4z1nVGajyu5Y130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261557.RAJUwBs4HfghWZjD8PI2I5GEK8mbLnQFO4z1nVGajyu5Y130_provenance.
• NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_provenance.
• NP1359070.RABDU-mjsy71hHcdtsF7o4WrLzOKoeywuWvlpLGawawg0130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1359070.RABDU-mjsy71hHcdtsF7o4WrLzOKoeywuWvlpLGawawg0130_provenance.
• assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP220350.RAMJhhXmNViCtC9xi3rBFQBiVC7SSFgF4OKAxutALf5K0130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220350.RAMJhhXmNViCtC9xi3rBFQBiVC7SSFgF4OKAxutALf5K0130_provenance.
• NP1359069.RAFGG2s7IOytS-x2uAu8FmcERVcdrw1AS9OBG0PEf47Ew130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1359069.RAFGG2s7IOytS-x2uAu8FmcERVcdrw1AS9OBG0PEf47Ew130_provenance.
• NP300436.RAvU5qFd1xuMzlE-nQEVLtJjOSEnK2id64cSn1-RUfEx0130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300436.RAvU5qFd1xuMzlE-nQEVLtJjOSEnK2id64cSn1-RUfEx0130_provenance.
• NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.