Matches in Nanopublications for { ?s ?p "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- NP535117.RA7EUpWw0Pzqooke8prqm6pFFvoW2Lb4mkKJtLRtTJOCU130_assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535117.RA7EUpWw0Pzqooke8prqm6pFFvoW2Lb4mkKJtLRtTJOCU130_provenance.
- assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.