Matches in Nanopublications for { ?s ?p "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP894706.RAeKImviRtmdpV6Ci6cncZ4PBXYMr4r7XQzGykTZcwSDM130_assertion description "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894706.RAeKImviRtmdpV6Ci6cncZ4PBXYMr4r7XQzGykTZcwSDM130_provenance.
- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion description "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_provenance.
- assertion description "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP724562.RA-Bg_CuwB6xRydCqinNattT7TEpbLnIQkFFEu0ikQsUU130_assertion description "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724562.RA-Bg_CuwB6xRydCqinNattT7TEpbLnIQkFFEu0ikQsUU130_provenance.