Matches in Nanopublications for { ?s ?p "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_provenance.
- assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP592060.RADt8FAF-2QZcqHSATxSdPMsCvtNv8xaeyG5_SdBjLeZc130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592060.RADt8FAF-2QZcqHSATxSdPMsCvtNv8xaeyG5_SdBjLeZc130_provenance.
- assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_provenance.
- NP879140.RAvgPgqZ3IeiwQp3LPL8bYxPG54SF8Htm8gkntscIH5KM130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879140.RAvgPgqZ3IeiwQp3LPL8bYxPG54SF8Htm8gkntscIH5KM130_provenance.
- NP592062.RAtzCc9N-k1LO10qKF4B98vbpNB7MjntSALjAKokUjFg0130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592062.RAtzCc9N-k1LO10qKF4B98vbpNB7MjntSALjAKokUjFg0130_provenance.
- NP592057.RAKvKyOn1Ec-TC69-6F-lI5AtO08gqjLiTTAYpjiA2fkc130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592057.RAKvKyOn1Ec-TC69-6F-lI5AtO08gqjLiTTAYpjiA2fkc130_provenance.
- NP976666.RAEUrklBMgPZxVht_z_m0XN0kYUrZhqOG8orP0fDG9j3o130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976666.RAEUrklBMgPZxVht_z_m0XN0kYUrZhqOG8orP0fDG9j3o130_provenance.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_provenance.
- NP592064.RA3teGTlCsnwg8E41wyuaalrAyHLFpOcv7KwDzkxlO35A130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592064.RA3teGTlCsnwg8E41wyuaalrAyHLFpOcv7KwDzkxlO35A130_provenance.