Title: Familial hypomelanosis of Ito: Implications for genetic counselling
Abstract: American Journal of Medical GeneticsVolume 95, Issue 1 p. 82-84 Letter to the Editor Familial hypomelanosis of Ito: Implications for genetic counselling Martino Ruggieri, Corresponding Author Martino Ruggieri [email protected] Division of Paediatric Neurology, Department of Paediatrics, University of Catania, and IBFSNC, National Research Council (CNR), Catania, ItalyDivision of Paediatric Neurology, Department of Paediatrics, University of Catania, Via S. Sofia, 78, Catania, ItalySearch for more papers by this author Martino Ruggieri, Corresponding Author Martino Ruggieri [email protected] Division of Paediatric Neurology, Department of Paediatrics, University of Catania, and IBFSNC, National Research Council (CNR), Catania, ItalyDivision of Paediatric Neurology, Department of Paediatrics, University of Catania, Via S. Sofia, 78, Catania, ItalySearch for more papers by this author First published: 07 November 2000 https://doi.org/10.1002/1096-8628(20001106)95:1<82::AID-AJMG17>3.0.CO;2-LCitations: 16Read 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 Amon M, Menapace R, Kirnbauer R 1990. Ocular symptomatology in familial hypomelanosis of Ito. Ophthalmologica 200: 1–6. 10.1159/000310069 CASPubMedWeb of Science®Google Scholar Bodemer C, Rotig A, Rustin P. 1999. Hair and skin disorders as signs of mitochondrial disease. 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Publication Year: 2000
Publication Date: 2000-11-06
Language: en
Type: article
Indexed In: ['crossref']
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Cited By Count: 1
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