Matches in Nanopublications for { ?s ?p "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_provenance.
- assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_provenance.
- NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622592.RAFCwJL1UC1D1aTdyWA7UGw5vX72hSFokrlIfGCeAzG7g130_provenance.
- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_provenance.