FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2090410554> ?p ?o ?g. }

• W2090410554 endingPage "187" @default.
• W2090410554 startingPage "184" @default.
• W2090410554 abstract "Pediatrics InternationalVolume 46, Issue 2 p. 184-187 Atypical crossed polydactyly in two siblings with Ellis-van Creveld Syndrome and mild clinical manifestations in close relatives Aysenur Ökten, Aysenur Ökten Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this authorMurat Çakir, Murat Çakir Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this authorFazil Orhan, Fazil Orhan Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this authorIlke Mungan, Ilke Mungan Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this author Aysenur Ökten, Aysenur Ökten Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this authorMurat Çakir, Murat Çakir Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this authorFazil Orhan, Fazil Orhan Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this authorIlke Mungan, Ilke Mungan Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, Trabzon, TurkeySearch for more papers by this author First published: 05 April 2004 https://doi.org/10.1046/j.1442-200x.2004.01871.xCitations: 2 Murat Çakir MD, Department of Pediatrics, Karadeniz Technical University Faculty of Medicine, 61080 Trabzon, Turkey. Email: [email protected] 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 onEmailFacebookTwitterLinkedInRedditWechat References 1 Temtamy SA, McKusick VA. The genetics of hand malformations. Birth Defects Orig. Artic. Series 1978; 14: i−xviii, 1 −619 . 2 Nathan PA, Keniston RC. Crossed polydactyly. Case report and review of the literature. J. Bone Joint Surg. Am. 1975; 57: 847−9. 3 Da Silva EO, Janovitz D, De Albuquerque SC. Ellis-van Creveld syndrome: report of 15 cases in an inbred kindred. J. Med. Genet. 1980; 17: 349−56. 4 Polymeropoulos MH, Ide SE, Wright M et al. The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16. Genomics 1996; 35: 1−5. 5 McKusick VA. Ellis-van Creveld syndrome and the Amish. Nat. Genet. 2000; 24: 203−4. 6 Ruiz-Perez VL, Tompson SW, Blair HJ et al. Mutations in two nonhomologous genes in a head-to-head configuration cause Ellis-van Creveld syndrome. Am. J. Hum. Genet. 2003; 72: 728−32. 7 Susami T, Kuroda T, Yoshimasu H, Suzuki R. Ellis-van Creveld syndrome: craniofacial morphology and multidisciplinary treatment. Cleft Palate Craniofac. J. 1999; 36: 345−52. 8 Katsouras CS, Thomadakis C, Michalis LK. Cardiac Ellis-van Creveld syndrome. Int. J. Cardiol. 2003; 87: 315−16. 9 Rosemberg S, Carneiro PC, Zerbini MC, Gonzalez CH. Brief clinical report: chondroectodermal dysplasia (Ellis-van Creveld) with anomalies of CNS and urinary tract. Am. J. Med. Genet. 1983; 15: 291−5. 10 Fryns JP. Postaxial polydactyly as heterozygote manifestation in Ellis-Van Creveld syndrome? Am. J. Med. Genet. 1991; 39: 500−1. 11 Howard TD, Guttmacher AE, McKinnon W, Sharma M, McKusick VA, Jabs EW. Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus. Am. J. Hum. Genet. 1997; 61: 1405−12. 12 Hayashi M, Takagi T, Masada Y. Lateral ray polydactyly: a case of duplicated metatarsal with normal phalanges. Ann. Plast. Surg. 1997; 39: 97−9. 13 Aydingoz U, Cila A, Aktan G. Rhombencephalosynapsis associated with hand anomalies. Br. J. Radiol. 1997; 70: 764−6. 14 Blauth W, Olason AT. Classification of polydactyly of the hands and feet. Arch. Orthop. Trauma Surg. 1988; 107: 334−44. Citing Literature Volume46, Issue2April 2004Pages 184-187 ReferencesRelatedInformation" @default.
• W2090410554 created "2016-06-24" @default.
• W2090410554 creator A5012456970 @default.
• W2090410554 creator A5022181509 @default.
• W2090410554 creator A5065676166 @default.
• W2090410554 creator A5073594505 @default.
• W2090410554 date "2004-04-01" @default.
• W2090410554 modified "2023-10-17" @default.
• W2090410554 title "Atypical crossed polydactyly in two siblings with Ellis-van Creveld Syndrome and mild clinical manifestations in close relatives" @default.
• W2090410554 cites W1964936160 @default.
• W2090410554 cites W1991532564 @default.
• W2090410554 cites W1992895234 @default.
• W2090410554 cites W2000520592 @default.
• W2090410554 cites W2003454627 @default.
• W2090410554 cites W2030572098 @default.
• W2090410554 cites W2035801879 @default.
• W2090410554 cites W2043759352 @default.
• W2090410554 cites W2058089655 @default.
• W2090410554 cites W2103415909 @default.
• W2090410554 cites W2157544977 @default.
• W2090410554 cites W2337897940 @default.
• W2090410554 cites W4229799536 @default.
• W2090410554 doi "https://doi.org/10.1046/j.1442-200x.2004.01871.x" @default.
• W2090410554 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15056248" @default.
• W2090410554 hasPublicationYear "2004" @default.
• W2090410554 type Work @default.
• W2090410554 sameAs 2090410554 @default.
• W2090410554 citedByCount "2" @default.
• W2090410554 crossrefType "journal-article" @default.
• W2090410554 hasAuthorship W2090410554A5012456970 @default.
• W2090410554 hasAuthorship W2090410554A5022181509 @default.
• W2090410554 hasAuthorship W2090410554A5065676166 @default.
• W2090410554 hasAuthorship W2090410554A5073594505 @default.
• W2090410554 hasBestOaLocation W20904105541 @default.
• W2090410554 hasConcept C161191863 @default.
• W2090410554 hasConcept C187212893 @default.
• W2090410554 hasConcept C2986411436 @default.
• W2090410554 hasConcept C3017595490 @default.
• W2090410554 hasConcept C41008148 @default.
• W2090410554 hasConcept C512399662 @default.
• W2090410554 hasConcept C71924100 @default.
• W2090410554 hasConceptScore W2090410554C161191863 @default.
• W2090410554 hasConceptScore W2090410554C187212893 @default.
• W2090410554 hasConceptScore W2090410554C2986411436 @default.
• W2090410554 hasConceptScore W2090410554C3017595490 @default.
• W2090410554 hasConceptScore W2090410554C41008148 @default.
• W2090410554 hasConceptScore W2090410554C512399662 @default.
• W2090410554 hasConceptScore W2090410554C71924100 @default.
• W2090410554 hasIssue "2" @default.
• W2090410554 hasLocation W20904105541 @default.
• W2090410554 hasLocation W20904105542 @default.
• W2090410554 hasOpenAccess W2090410554 @default.
• W2090410554 hasPrimaryLocation W20904105541 @default.
• W2090410554 hasRelatedWork W2011669067 @default.
• W2090410554 hasRelatedWork W2039411811 @default.
• W2090410554 hasRelatedWork W2440024666 @default.
• W2090410554 hasRelatedWork W2601862538 @default.
• W2090410554 hasRelatedWork W3194609374 @default.
• W2090410554 hasRelatedWork W4237821059 @default.
• W2090410554 hasRelatedWork W4288046443 @default.
• W2090410554 hasRelatedWork W4293180912 @default.
• W2090410554 hasRelatedWork W4318482388 @default.
• W2090410554 hasRelatedWork W2611037281 @default.
• W2090410554 hasVolume "46" @default.
• W2090410554 isParatext "false" @default.
• W2090410554 isRetracted "false" @default.
• W2090410554 magId "2090410554" @default.
• W2090410554 workType "article" @default.