Matches in Nanopublications for { ?s ?p "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP733645.RAA_LPux2IG3YilfkUe8NAbdwJDX7WIvjQ_s2YUQoYVFY130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733645.RAA_LPux2IG3YilfkUe8NAbdwJDX7WIvjQ_s2YUQoYVFY130_provenance.
- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_provenance.
- assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_provenance.
- NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_provenance.
- NP658029.RA5Z_IhqQsEb4WfPydfgAgdAvwTAqHAEMY3CysqOIMrKc130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658029.RA5Z_IhqQsEb4WfPydfgAgdAvwTAqHAEMY3CysqOIMrKc130_provenance.