Matches in Nanopublications for { ?s ?p "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1866.RATMh6lTvKB3SSo1rwdoEcjV0UNMDhfAPIw_dCf61JxW4130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1866.RATMh6lTvKB3SSo1rwdoEcjV0UNMDhfAPIw_dCf61JxW4130_provenance.
- NP602472.RAjVA9rd7Yigzok6wK2xGyUs3fzA9qzmp34zp8gkwVwKQ130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602472.RAjVA9rd7Yigzok6wK2xGyUs3fzA9qzmp34zp8gkwVwKQ130_provenance.
- NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843761.RAu59dN6WEigb5D2GJtDRjTjcWX2P5Ek_sD9mPY7i48Z8130_provenance.
- NP4114.RA3AFCIu_AgMF4d5OouMkVSZCIOuwxTB0aCMiAAveBCNQ130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4114.RA3AFCIu_AgMF4d5OouMkVSZCIOuwxTB0aCMiAAveBCNQ130_provenance.
- NP944911.RAw7gDTzMKfAjl9vzTqUgcuGIHr9nYVM_v4y2Y5i90ILo130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944911.RAw7gDTzMKfAjl9vzTqUgcuGIHr9nYVM_v4y2Y5i90ILo130_provenance.
- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_provenance.
- NP7387.RA_1cCrdB2Pc-6IHpzSsZIY4JsXmekiNhST_dM3kZV4a0130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7387.RA_1cCrdB2Pc-6IHpzSsZIY4JsXmekiNhST_dM3kZV4a0130_provenance.
- NP1057469.RAw2FexgTFacqmU90uTNjj30OnVrzhLgxvd6XWPwlP4UM130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057469.RAw2FexgTFacqmU90uTNjj30OnVrzhLgxvd6XWPwlP4UM130_provenance.
- assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1057468.RAIn-CoJ4LsQ_LK4VG6WxUXvzgQb8OrZ4TmGs6cPMdygs130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057468.RAIn-CoJ4LsQ_LK4VG6WxUXvzgQb8OrZ4TmGs6cPMdygs130_provenance.