DERMATOGLYPHIC ANALYSES OF 24 INDIVIDUALS WITH THE PRADER-WILLI SYNDROME
1982; Wiley; Volume: 26; Issue: 2 Linguagem: Inglês
10.1111/j.1365-2788.1982.tb00132.x
ISSN1365-2788
AutoresArabella Smith, Eunice Simpson,
Tópico(s)Dermatoglyphics and Human Traits
ResumoJournal of Intellectual Disability ResearchVolume 26, Issue 2 p. 91-99 DERMATOGLYPHIC ANALYSES OF 24 INDIVIDUALS WITH THE PRADER-WILLI SYNDROME Arabella Smith, Arabella Smith Cytogenetics Unit, Oliver Latham Laboratory, Health Commission of New South Wales Sydney, AustraliaSearch for more papers by this authorEunice Simpson, Eunice Simpson Cytogenetics Unit, Oliver Latham Laboratory, Health Commission of New South Wales Sydney, AustraliaSearch for more papers by this author Arabella Smith, Arabella Smith Cytogenetics Unit, Oliver Latham Laboratory, Health Commission of New South Wales Sydney, AustraliaSearch for more papers by this authorEunice Simpson, Eunice Simpson Cytogenetics Unit, Oliver Latham Laboratory, Health Commission of New South Wales Sydney, AustraliaSearch for more papers by this author First published: June 1982 https://doi.org/10.1111/j.1365-2788.1982.tb00132.xCitations: 3AboutPDF 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. 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