Matches in Nanopublications for { ?s ?p "[The infant was found to be heterozygous for the prothrombin G20210A mutation and homozygous for the methylenetetrahydrofolate reductase C667T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP415065.RATTCkaDfhSjv8YBbM8xolE7vCnSHYh7fEEUma3mtLew8130_assertion description "[The infant was found to be heterozygous for the prothrombin G20210A mutation and homozygous for the methylenetetrahydrofolate reductase C667T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415065.RATTCkaDfhSjv8YBbM8xolE7vCnSHYh7fEEUma3mtLew8130_provenance.
- NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_assertion description "[The infant was found to be heterozygous for the prothrombin G20210A mutation and homozygous for the methylenetetrahydrofolate reductase C667T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411961.RAq0uSt0_aoU8twp9gua4e4mvkxfDUQ9aij6ggApwpFtY130_provenance.
- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion description "[The infant was found to be heterozygous for the prothrombin G20210A mutation and homozygous for the methylenetetrahydrofolate reductase C667T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_provenance.