Matches in Nanopublications for { ?s ?p "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP20733.RAtP_SpVfMZH7hnbWa2U7IdDdnYeIc1uXDh-0c2kGVTbQ130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20733.RAtP_SpVfMZH7hnbWa2U7IdDdnYeIc1uXDh-0c2kGVTbQ130_provenance.
- NP20042.RAadhuyVT-gMa81IgVjm5Gmqtir9xrTYpLbDuh4Ppt1r8130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20042.RAadhuyVT-gMa81IgVjm5Gmqtir9xrTYpLbDuh4Ppt1r8130_provenance.
- NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20044.RAwqBp2XHJiR5zNg576ISxRU9C9jOoEdWoV2-HbL5MoHo130_provenance.
- assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP983908.RAhLwVDPtZxzZHwiPznmcdgZvcB1CVQCxJ8DjbRz7rYso130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983908.RAhLwVDPtZxzZHwiPznmcdgZvcB1CVQCxJ8DjbRz7rYso130_provenance.
- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_provenance.
- NP31277.RAHEuj2zf5FSAZpO9Ox0V_qHZVic5xqyBNmx_hKPYZ6nA130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31277.RAHEuj2zf5FSAZpO9Ox0V_qHZVic5xqyBNmx_hKPYZ6nA130_provenance.
- NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31278.RAMfHqAMtSEhtm1Vl7CXI948o2IN8wPihQ3inoYUx-__s130_provenance.
- NP31280.RAK-PZedSG0qftecG_QaNhQBdzHMV74xNlIWQnJiTY96A130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31280.RAK-PZedSG0qftecG_QaNhQBdzHMV74xNlIWQnJiTY96A130_provenance.
- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_provenance.