Matches in Nanopublications for { ?s ?p "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP408454.RAgXiuGx0K3OGTHwqeefEse_c_V5xeLx24FuOilBraOPc130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408454.RAgXiuGx0K3OGTHwqeefEse_c_V5xeLx24FuOilBraOPc130_provenance.
- assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- NP908152.RAfbQYhRhNtBmq1_0Z58IGoQTHel5c5kljRTk0K0zxcCs130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908152.RAfbQYhRhNtBmq1_0Z58IGoQTHel5c5kljRTk0K0zxcCs130_provenance.
- NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409235.RAofKLeEp7m8ORElf7gTEVL2-wKvQpCL3JV4af80TLW-w130_provenance.
- NP807692.RAPGg_Sa4xWBApk88iUV-ygFZWwsb3afkvCSWpxBG4Xf4130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807692.RAPGg_Sa4xWBApk88iUV-ygFZWwsb3afkvCSWpxBG4Xf4130_provenance.
- NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.