Matches in Nanopublications for { ?s ?p "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP723212.RAz7rrUB0OMfNyb5lL1ZTicqLUPGqQc8Cg3gsaTDblihg130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723212.RAz7rrUB0OMfNyb5lL1ZTicqLUPGqQc8Cg3gsaTDblihg130_provenance.
- NP723402.RACVOqT6NJ4qWJQR1b4AcdZefMze5jsEi6QyOzZPhhUhE130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723402.RACVOqT6NJ4qWJQR1b4AcdZefMze5jsEi6QyOzZPhhUhE130_provenance.
- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_provenance.
- NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353260.RA1EV9yM7Qj17uhn1Mhls5ZNv6C9L71L9XSCU2JwmXHH4130_provenance.
- NP723334.RAYt7Vdol1n8YGew7ypSJzfPF0GOWCM693W7Aejp5Oj60130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723334.RAYt7Vdol1n8YGew7ypSJzfPF0GOWCM693W7Aejp5Oj60130_provenance.
- assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP834381.RAyJjY5wGdnDWqDUSYEspwdrt9hocPZ2N7a9x8P7lHYW4130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834381.RAyJjY5wGdnDWqDUSYEspwdrt9hocPZ2N7a9x8P7lHYW4130_provenance.
- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_provenance.
- assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.