Stüve-Wiedemann syndrome: Update and historical footnote

1996; Wiley; Volume: 63; Issue: 1 Linguagem: Inglês

10.1002/(sici)1096-8628(19960503)63

ISSN

1096-8628

Autores

H. ‐R. Wiedemann, Annemarie Stüve,

Tópico(s)

Gender Studies in Language

Resumo

American Journal of Medical GeneticsVolume 63, Issue 1 p. 12-16 Skeletal Dysplasia: Clinical and Radiological Aspects Stüve-Wiedemann syndrome: Update and historical footnote Hans-Rudolf Wiedemann, Corresponding Author Hans-Rudolf Wiedemann Department of Pediatrics, Christian-Albrechts Universität, Kiel, GermanyUniversitäts-Kinderklinik, Schwanenweg 20, D-24105 Kiel, GermanySearch for more papers by this authorAnnemarie Stüve, Annemarie Stüve Department of Pediatrics, Naunhof, GermanySearch for more papers by this author Hans-Rudolf Wiedemann, Corresponding Author Hans-Rudolf Wiedemann Department of Pediatrics, Christian-Albrechts Universität, Kiel, GermanyUniversitäts-Kinderklinik, Schwanenweg 20, D-24105 Kiel, GermanySearch for more papers by this authorAnnemarie Stüve, Annemarie Stüve Department of Pediatrics, Naunhof, GermanySearch for more papers by this author First published: 3 May 1996 https://doi.org/10.1002/(SICI)1096-8628(19960503)63:1 3.0.CO;2-UCitations: 21AboutPDF 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 Abstract Stüve-Wiedemann syndrome (SWS) is, at last, beginning to emerge from the shadows of campomelic syndrome as a nosologically and, presumably, causally-distinct entity, first delineated in 1971 on the basis of 2 affected sisters. The fact that these sisters had an affected double first cousin supports autosomal-recessive inheritance of SWS. © 1996 Wiley-Liss, Inc. Citing Literature Volume63, Issue13 May 1996Pages 12-16 RelatedInformation

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