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- NP916543.RASYkidcUzXeU5chcsJIbp98ajKGuuO7CGdpTFZnrQzQk130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916543.RASYkidcUzXeU5chcsJIbp98ajKGuuO7CGdpTFZnrQzQk130_provenance.
- NP14371.RAaI5VWplX31McgO9q3tRpSnnp83eaNBdYoM4UU-MHGG0130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14371.RAaI5VWplX31McgO9q3tRpSnnp83eaNBdYoM4UU-MHGG0130_provenance.
- assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP23981.RAeUu9hOrun0kW3OLwPo6OFI4t_vggbqCYeVhlaRseoeY130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23981.RAeUu9hOrun0kW3OLwPo6OFI4t_vggbqCYeVhlaRseoeY130_provenance.
- NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- NP735693.RAFbdzz1zwOPsGICdRNBkELKZt2i9pBV7jsh4geUxzQJ8130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735693.RAFbdzz1zwOPsGICdRNBkELKZt2i9pBV7jsh4geUxzQJ8130_provenance.
- NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.