Matches in Nanopublications for { ?s ?p "[Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_assertion description "[Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion description "[Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_provenance.