Matches in Nanopublications for { ?s ?p "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 14 of
14
with 100 items per page.
- NP45110.RARadVbCvA2zZzsXkK0McHrg-mOEr5cHkYd0_7RSVqPEw130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45110.RARadVbCvA2zZzsXkK0McHrg-mOEr5cHkYd0_7RSVqPEw130_provenance.
- assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49327.RAxqI-NoLkGw438uBqQ3duU5ozCqoJACOm27c_9mBSees130_provenance.
- assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP4554.RARMzY3OJMEHmo8KvKCFKRPNYnS754bQpco-XjCw9RBu4130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4554.RARMzY3OJMEHmo8KvKCFKRPNYnS754bQpco-XjCw9RBu4130_provenance.
- NP1799.RAH_SthMzMjLbC2EvS9wX5_aKb17ZYUYb76T8iDf-2wV0130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1799.RAH_SthMzMjLbC2EvS9wX5_aKb17ZYUYb76T8iDf-2wV0130_provenance.
- NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2457.RAAovslGwUwt1SG2nYdZgdZvvw_4fl6HRoraSM4F6v2bg130_provenance.
- NP53926.RA5W9YUxuUqR8b-sCdh4PzoegDTuW-P8ucERG-PJEBPog130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53926.RA5W9YUxuUqR8b-sCdh4PzoegDTuW-P8ucERG-PJEBPog130_provenance.
- NP4555.RAo4T5NKHAJpEQZZoxFI3StTVxtna9W2WMEwmJBb1oT5I130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4555.RAo4T5NKHAJpEQZZoxFI3StTVxtna9W2WMEwmJBb1oT5I130_provenance.
- NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP60602.RAGG902l1OQtW_-6i5uEv9OCvKzuTEctxGHgW-g5Ue9u4130_provenance.
- NP100932.RAJTViJ5UmMneBelwmvuW8-c5amNVyqbPyf-jUJfs9oyw130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100932.RAJTViJ5UmMneBelwmvuW8-c5amNVyqbPyf-jUJfs9oyw130_provenance.
- NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_assertion description "[Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100931.RAwXpnbOn8fkHzRDr6_JpEo2ggfVApUhptgj3goqe8RJ4130_provenance.