Matches in Nanopublications for { ?s ?p "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP2743.RAQa5WqoxHkzZrDQprmcLQ-ku3XTB2-u7V07eJCsND54o130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2743.RAQa5WqoxHkzZrDQprmcLQ-ku3XTB2-u7V07eJCsND54o130_provenance.
- NP295037.RAnOdXV6XhQ3AeubGaCdYH2TB9r5hM4XlWXAd7iafwS1A130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295037.RAnOdXV6XhQ3AeubGaCdYH2TB9r5hM4XlWXAd7iafwS1A130_provenance.
- assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP426450.RAYkFVkcNp34-jSMgSokAMKisQNP2qWHEhHo9HwWhMLi8130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426450.RAYkFVkcNp34-jSMgSokAMKisQNP2qWHEhHo9HwWhMLi8130_provenance.
- NP3703.RAab_GSbl6UfIuHKORbxMmAQZFo1R4jVnCXJ9dzp3EMhc130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3703.RAab_GSbl6UfIuHKORbxMmAQZFo1R4jVnCXJ9dzp3EMhc130_provenance.
- NP88483.RAXF8MZ-xdO8IwMcn9HHkzO-RTAPnd5O9mdW8VmNRWWps130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88483.RAXF8MZ-xdO8IwMcn9HHkzO-RTAPnd5O9mdW8VmNRWWps130_provenance.
- NP106343.RABV3xDnX6JxYL8bPqePlhF-M8tV66o8WeGlxz2T92jlQ130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106343.RABV3xDnX6JxYL8bPqePlhF-M8tV66o8WeGlxz2T92jlQ130_provenance.
- NP464376.RAssbI9PVlOlk_Cx5Dzhc0kr-lx-ZxB-MQhUM3_McyA-4130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464376.RAssbI9PVlOlk_Cx5Dzhc0kr-lx-ZxB-MQhUM3_McyA-4130_provenance.
- NP139553.RAJwKag66uTOqBE7JcioiByEZcWQRA5_BwyUlgLvoH8Hg130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139553.RAJwKag66uTOqBE7JcioiByEZcWQRA5_BwyUlgLvoH8Hg130_provenance.
- NP88484.RA5M37Px1yi1tCAJF7577dh4etVjaD7u5yfmlKolNRJuc130_assertion description "[Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88484.RA5M37Px1yi1tCAJF7577dh4etVjaD7u5yfmlKolNRJuc130_provenance.