Matches in Nanopublications for { ?s ?p "[Using cloned fragments from the myotonic dystrophy (DM) and fragile X syndrome (FRAXA) loci containing normal, premutation, and full mutation lengths of repeats, we report the formation of novel alternative DNA secondary structures that map within the repeat tracts during reannealing of complementary strands, containing equal lengths of repeats, into linear duplex DNA molecules.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP665967.RAfOPr8vnj5lmHKMHac4YcoX694v5hMfyuH2_xqL-cu3k130_assertion description "[Using cloned fragments from the myotonic dystrophy (DM) and fragile X syndrome (FRAXA) loci containing normal, premutation, and full mutation lengths of repeats, we report the formation of novel alternative DNA secondary structures that map within the repeat tracts during reannealing of complementary strands, containing equal lengths of repeats, into linear duplex DNA molecules.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665967.RAfOPr8vnj5lmHKMHac4YcoX694v5hMfyuH2_xqL-cu3k130_provenance.
- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion description "[Using cloned fragments from the myotonic dystrophy (DM) and fragile X syndrome (FRAXA) loci containing normal, premutation, and full mutation lengths of repeats, we report the formation of novel alternative DNA secondary structures that map within the repeat tracts during reannealing of complementary strands, containing equal lengths of repeats, into linear duplex DNA molecules.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_provenance.