Matches in Nanopublications for { ?s ?p "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_provenance.
- NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_provenance.
- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_provenance.
- assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_provenance.