Matches in SemOpenAlex for { <https://semopenalex.org/work/W2128185904> ?p ?o ?g. }
Showing items 1 to 85 of
85
with 100 items per page.
- W2128185904 endingPage "609" @default.
- W2128185904 startingPage "608" @default.
- W2128185904 abstract "American Journal of Medical Genetics Part AVolume 143A, Issue 6 p. 608-609 Research Letter X-linked retinoschisis in a female with a heterozygous RS1 missense mutation† Manuel Saldana, Manuel Saldana Department of Ophthalmology, Leeds General Infirmary, Leeds, United KingdomSearch for more papers by this authorJenny Thompson, Jenny Thompson Department of Clinical Genetics, St James University Hospital, Leeds, United KingdomSearch for more papers by this authorElizabeth Monk, Elizabeth Monk Molecular Genetics Laboratory, Addenbrookes Hospital, Cambridge, United KingdomSearch for more papers by this authorDorothy Trump, Dorothy Trump Academic Unit of Medical Genetics, School of Medicine & Centre for Molecular Medicine, Faculty of Medical Health Sciences and Regional Genetics Services, St Mary's Hospital, Manchester, United KingdomSearch for more papers by this authorVernon Long, Vernon Long Department of Ophthalmology, Leeds General Infirmary, Leeds, United KingdomSearch for more papers by this authorEamonn Sheridan, Corresponding Author Eamonn Sheridan eamonn.sheridan@leedsth.nhs.uk Department of Clinical Genetics, St James University Hospital, Leeds, United KingdomConsultant in Clinical Genetics, Yorkshire Regional Genetics Service, Ashley Wing, St James's University Hospital, Leeds Teaching Hospitals, Leeds LS9 7TF, UK.Search for more papers by this author Manuel Saldana, Manuel Saldana Department of Ophthalmology, Leeds General Infirmary, Leeds, United KingdomSearch for more papers by this authorJenny Thompson, Jenny Thompson Department of Clinical Genetics, St James University Hospital, Leeds, United KingdomSearch for more papers by this authorElizabeth Monk, Elizabeth Monk Molecular Genetics Laboratory, Addenbrookes Hospital, Cambridge, United KingdomSearch for more papers by this authorDorothy Trump, Dorothy Trump Academic Unit of Medical Genetics, School of Medicine & Centre for Molecular Medicine, Faculty of Medical Health Sciences and Regional Genetics Services, St Mary's Hospital, Manchester, United KingdomSearch for more papers by this authorVernon Long, Vernon Long Department of Ophthalmology, Leeds General Infirmary, Leeds, United KingdomSearch for more papers by this authorEamonn Sheridan, Corresponding Author Eamonn Sheridan eamonn.sheridan@leedsth.nhs.uk Department of Clinical Genetics, St James University Hospital, Leeds, United KingdomConsultant in Clinical Genetics, Yorkshire Regional Genetics Service, Ashley Wing, St James's University Hospital, Leeds Teaching Hospitals, Leeds LS9 7TF, UK.Search for more papers by this author First published: 22 February 2007 https://doi.org/10.1002/ajmg.a.31568Citations: 13 † How to cite this article: Saldana M, Thompson J, Monk E, Trump D, Long V, Sheridan E. 2007. X-linked retinoschisis in a female with a heterozygous RS1 missense mutation. Am J Med Genet Part A 143A:608–609. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume143A, Issue615 March 2007Pages 608-609 RelatedInformation" @default.
- W2128185904 created "2016-06-24" @default.
- W2128185904 creator A5015231107 @default.
- W2128185904 creator A5023696132 @default.
- W2128185904 creator A5029028452 @default.
- W2128185904 creator A5045064606 @default.
- W2128185904 creator A5055154281 @default.
- W2128185904 creator A5071239634 @default.
- W2128185904 date "2007-02-22" @default.
- W2128185904 modified "2023-10-13" @default.
- W2128185904 title "X-linked retinoschisis in a female with a heterozygousRS1 missense mutation" @default.
- W2128185904 cites W1512026426 @default.
- W2128185904 cites W1974019768 @default.
- W2128185904 cites W2000249838 @default.
- W2128185904 cites W2040265757 @default.
- W2128185904 cites W2042534215 @default.
- W2128185904 cites W2080270797 @default.
- W2128185904 cites W2092191261 @default.
- W2128185904 cites W2092724715 @default.
- W2128185904 cites W2130950303 @default.
- W2128185904 cites W51356833 @default.
- W2128185904 doi "https://doi.org/10.1002/ajmg.a.31568" @default.
- W2128185904 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17304551" @default.
- W2128185904 hasPublicationYear "2007" @default.
- W2128185904 type Work @default.
- W2128185904 sameAs 2128185904 @default.
- W2128185904 citedByCount "19" @default.
- W2128185904 countsByYear W21281859042012 @default.
- W2128185904 countsByYear W21281859042014 @default.
- W2128185904 countsByYear W21281859042016 @default.
- W2128185904 countsByYear W21281859042017 @default.
- W2128185904 countsByYear W21281859042019 @default.
- W2128185904 countsByYear W21281859042020 @default.
- W2128185904 countsByYear W21281859042021 @default.
- W2128185904 countsByYear W21281859042022 @default.
- W2128185904 countsByYear W21281859042023 @default.
- W2128185904 crossrefType "journal-article" @default.
- W2128185904 hasAuthorship W2128185904A5015231107 @default.
- W2128185904 hasAuthorship W2128185904A5023696132 @default.
- W2128185904 hasAuthorship W2128185904A5029028452 @default.
- W2128185904 hasAuthorship W2128185904A5045064606 @default.
- W2128185904 hasAuthorship W2128185904A5055154281 @default.
- W2128185904 hasAuthorship W2128185904A5071239634 @default.
- W2128185904 hasConcept C104317684 @default.
- W2128185904 hasConcept C118487528 @default.
- W2128185904 hasConcept C161191863 @default.
- W2128185904 hasConcept C41008148 @default.
- W2128185904 hasConcept C512399662 @default.
- W2128185904 hasConcept C54355233 @default.
- W2128185904 hasConcept C64474127 @default.
- W2128185904 hasConcept C71924100 @default.
- W2128185904 hasConcept C74909509 @default.
- W2128185904 hasConcept C86803240 @default.
- W2128185904 hasConceptScore W2128185904C104317684 @default.
- W2128185904 hasConceptScore W2128185904C118487528 @default.
- W2128185904 hasConceptScore W2128185904C161191863 @default.
- W2128185904 hasConceptScore W2128185904C41008148 @default.
- W2128185904 hasConceptScore W2128185904C512399662 @default.
- W2128185904 hasConceptScore W2128185904C54355233 @default.
- W2128185904 hasConceptScore W2128185904C64474127 @default.
- W2128185904 hasConceptScore W2128185904C71924100 @default.
- W2128185904 hasConceptScore W2128185904C74909509 @default.
- W2128185904 hasConceptScore W2128185904C86803240 @default.
- W2128185904 hasIssue "6" @default.
- W2128185904 hasLocation W21281859041 @default.
- W2128185904 hasLocation W21281859042 @default.
- W2128185904 hasOpenAccess W2128185904 @default.
- W2128185904 hasPrimaryLocation W21281859041 @default.
- W2128185904 hasRelatedWork W1970285803 @default.
- W2128185904 hasRelatedWork W2021002294 @default.
- W2128185904 hasRelatedWork W2035623498 @default.
- W2128185904 hasRelatedWork W2135206290 @default.
- W2128185904 hasRelatedWork W2150627712 @default.
- W2128185904 hasRelatedWork W2588250610 @default.
- W2128185904 hasRelatedWork W3144426676 @default.
- W2128185904 hasRelatedWork W4240870703 @default.
- W2128185904 hasRelatedWork W4244538220 @default.
- W2128185904 hasRelatedWork W972120878 @default.
- W2128185904 hasVolume "143A" @default.
- W2128185904 isParatext "false" @default.
- W2128185904 isRetracted "false" @default.
- W2128185904 magId "2128185904" @default.
- W2128185904 workType "article" @default.