Matches in Nanopublications for { ?s ?p "[Known genetic defects were excluded by performing autosomal recessive retinitis pigmentosa (arRP) genotyping microarray analysis and by Sanger sequencing of the coding exons and flanking intronic regions of eyes shut homolog-drosophila (EYS) and chromosome 2 open reading frame 71 (C2orf71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion description "[Known genetic defects were excluded by performing autosomal recessive retinitis pigmentosa (arRP) genotyping microarray analysis and by Sanger sequencing of the coding exons and flanking intronic regions of eyes shut homolog-drosophila (EYS) and chromosome 2 open reading frame 71 (C2orf71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_provenance.
- NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_assertion description "[Known genetic defects were excluded by performing autosomal recessive retinitis pigmentosa (arRP) genotyping microarray analysis and by Sanger sequencing of the coding exons and flanking intronic regions of eyes shut homolog-drosophila (EYS) and chromosome 2 open reading frame 71 (C2orf71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_assertion description "[Known genetic defects were excluded by performing autosomal recessive retinitis pigmentosa (arRP) genotyping microarray analysis and by Sanger sequencing of the coding exons and flanking intronic regions of eyes shut homolog-drosophila (EYS) and chromosome 2 open reading frame 71 (C2orf71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- NP907957.RAHiYpKcojJQYzdzn38IN_uJclzxPI_7500RRf_4D6ugI130_assertion description "[Known genetic defects were excluded by performing autosomal recessive retinitis pigmentosa (arRP) genotyping microarray analysis and by Sanger sequencing of the coding exons and flanking intronic regions of eyes shut homolog-drosophila (EYS) and chromosome 2 open reading frame 71 (C2orf71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907957.RAHiYpKcojJQYzdzn38IN_uJclzxPI_7500RRf_4D6ugI130_provenance.