Matches in Nanopublications for { ?s ?p "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP885431.RAhRRbpsGVoLXIogeGW_44WwQCrh4FdHkriecVIFIfRbE130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885431.RAhRRbpsGVoLXIogeGW_44WwQCrh4FdHkriecVIFIfRbE130_provenance.
- NP929027.RAoD0ia4Oq3BhyxVeyC4MQrcWDU-FD0zoMOXkI_j5zhr4130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929027.RAoD0ia4Oq3BhyxVeyC4MQrcWDU-FD0zoMOXkI_j5zhr4130_provenance.
- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_provenance.
- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_provenance.
- NP651642.RA78_RRJq_2yqZ2I4mgwwR62GADCyU5b0WNARMhXevbQE130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651642.RA78_RRJq_2yqZ2I4mgwwR62GADCyU5b0WNARMhXevbQE130_provenance.
- NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_provenance.
- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_provenance.
- NP810402.RArMBCWRvDQV7XO5qIn3kN2MdRf2A0cgThfSBrz8wilvo130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810402.RArMBCWRvDQV7XO5qIn3kN2MdRf2A0cgThfSBrz8wilvo130_provenance.
- NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536538.RAKYKlt4dOnr-0fkYdbJAonv0jatxVVIRzV9GkwJfaykI130_provenance.