Matches in Nanopublications for { ?s ?p "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600520.RAl-oKl8WAzG-6mijiqUeC_f4pOCD2UzLmQw4ioCFGUlY130_provenance.
- NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947448.RAA-5EQd_8nmlLGD7FVbUCx-Tq1y3sG2VcbordNpkK_iQ130_provenance.