Matches in Nanopublications for { ?s ?p "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_provenance.
- NP662512.RAdTZ9YH9E5YmYKPv2-1KvBdyfjliL1bP245Zazp9V7U8130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662512.RAdTZ9YH9E5YmYKPv2-1KvBdyfjliL1bP245Zazp9V7U8130_provenance.
- NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_provenance.
- NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_provenance.
- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_provenance.
- assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP600504.RAiqB74VEfCH3vFvII1xD7s5zZmelPOEPEHeSPV6FOAYA130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600504.RAiqB74VEfCH3vFvII1xD7s5zZmelPOEPEHeSPV6FOAYA130_provenance.
- NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354846.RAQ6FjTxLsuQpuSt7w8OgIuAOEWVgBM6ID-B1-TVz3Scs130_provenance.
- NP354847.RAZ3txcmQfTOuL5FTp27buYKYr_3xAD8dI6imEB8stbus130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354847.RAZ3txcmQfTOuL5FTp27buYKYr_3xAD8dI6imEB8stbus130_provenance.
- NP354848.RATsaM23P8FAMrnAuWcSFEEYjlt8a5zdttmsIkfE4Q81M130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354848.RATsaM23P8FAMrnAuWcSFEEYjlt8a5zdttmsIkfE4Q81M130_provenance.
- NP354845.RA5gH9_KFDkuGtviCm6ueJyzJdG6xHlOlVrSWeV7wEfmk130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354845.RA5gH9_KFDkuGtviCm6ueJyzJdG6xHlOlVrSWeV7wEfmk130_provenance.