Matches in Nanopublications for { ?s ?p "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_provenance.
- NP1029485.RA-XvvmJcqf9fj7hhjeSXTaQaIrsjg4BQzHjb5niWBIJE130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029485.RA-XvvmJcqf9fj7hhjeSXTaQaIrsjg4BQzHjb5niWBIJE130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.