Matches in Nanopublications for { ?s ?p "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1383184.RACcG-dFk3qxK2IlCJ8ZxT8Ah4IGk6Z3vG1eFsCsCDvPQ130_assertion description "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1383184.RACcG-dFk3qxK2IlCJ8ZxT8Ah4IGk6Z3vG1eFsCsCDvPQ130_provenance.
- NP782463.RAQCpTU2ogfP-nqxCwwSXMn6MI2QKoaVTbMHXuHkUJKkY130_assertion description "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782463.RAQCpTU2ogfP-nqxCwwSXMn6MI2QKoaVTbMHXuHkUJKkY130_provenance.
- assertion description "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_assertion description "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.