Matches in Nanopublications for { ?s ?p "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_provenance.
- NP850908.RA5fO5mgZhNUty-XUyQcfFzb163KfknDb5OaI1oDbPeag130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850908.RA5fO5mgZhNUty-XUyQcfFzb163KfknDb5OaI1oDbPeag130_provenance.
- assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302230.RA9M5sqmllyecD6-vWnv7LKvHEPj16n1hesaSV9s8Cvpc130_provenance.