Matches in Nanopublications for { ?s ?p "[We identified mutations in a new human gene, ESCO2, associated with Roberts syndrome in 15 kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP2040.RA-iCNQOV_I4TeR3_QRYXdZTnx3s19LzbxJCFzqlUSA24130_assertion description "[We identified mutations in a new human gene, ESCO2, associated with Roberts syndrome in 15 kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2040.RA-iCNQOV_I4TeR3_QRYXdZTnx3s19LzbxJCFzqlUSA24130_provenance.
- NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_assertion description "[We identified mutations in a new human gene, ESCO2, associated with Roberts syndrome in 15 kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_assertion description "[We identified mutations in a new human gene, ESCO2, associated with Roberts syndrome in 15 kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.