Matches in Nanopublications for { ?s ?p "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_assertion description "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3898.RAHIQ1wvI8jpHQa1rddIp455kkJICGYvJ79NqckSZeWrw130_provenance.
- NP588093.RAtY4L598h_QgX1C6NWrbOTOuQzaO-aklbIEiKZuiD2xw130_assertion description "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588093.RAtY4L598h_QgX1C6NWrbOTOuQzaO-aklbIEiKZuiD2xw130_provenance.
- NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_assertion description "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_assertion description "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5550.RA0u18rNblthwxhbvI4fSyRTcromovGdWkMV3GN2o6fZ0130_provenance.