Matches in Nanopublications for { ?s ?p "[We performed mutational analysis of MNX1 in all cases by DNA sequencing as well as by Multiplex Ligation-dependent Probe Amplification (MLPA) in those CS cases where no MNX1 mutations were found, to exclude a MNX1 heterozygous loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_assertion description "[We performed mutational analysis of MNX1 in all cases by DNA sequencing as well as by Multiplex Ligation-dependent Probe Amplification (MLPA) in those CS cases where no MNX1 mutations were found, to exclude a MNX1 heterozygous loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_assertion description "[We performed mutational analysis of MNX1 in all cases by DNA sequencing as well as by Multiplex Ligation-dependent Probe Amplification (MLPA) in those CS cases where no MNX1 mutations were found, to exclude a MNX1 heterozygous loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116302.RAnHYtj1N_yccEZCOSQUoJb_fNoMdzRU-srDt5spjLXhA130_provenance.