Matches in Nanopublications for { ?s ?p "[We used exome sequencing, Sanger sequencing, and copy number analysis to screen 65 unrelated individuals with schwannomatosis who were negative for a germline NF2 or SMARCB1 mutation.]. 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.
- assertion description "[We used exome sequencing, Sanger sequencing, and copy number analysis to screen 65 unrelated individuals with schwannomatosis who were negative for a germline NF2 or SMARCB1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion description "[We used exome sequencing, Sanger sequencing, and copy number analysis to screen 65 unrelated individuals with schwannomatosis who were negative for a germline NF2 or SMARCB1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_provenance.