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Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities

  • Published:1990-08 Issue:8 Volume:83 Page:531-532
  • ISSN:0141-0768
  • Container-title:Journal of the Royal Society of Medicine
  • language:en
  • Short-container-title:J R Soc Med

Author:

Bunker C B1,Atherton D2,Gray O P3,Tsioupra K4,Delhanty J D A4,Dowd P M1

Affiliation:

1. Department of Dermatology, University College and Middlesex School of Medicine, Mortimer Street, London W1N 8AA;

2. Department of Dermatology, The Hospitals for Sick Children, Great Ormond Street, London;

3. Department of Genetics and Biometry, University College, London;

4. Department of Child Health, Welsh National School of Medicine, Cardiff

Publisher

SAGE Publications

Subject

General Medicine

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial localized scleroderma with paediatric onset: a review;Advances in Dermatology and Allergology;2021

2. Aspects héréditaires et génétiques de la maladie de Raynaud;Journal des Maladies Vasculaires;2006-01

3. Primary Raynaud's phenomenon in monozygotic twins;Annals of the Rheumatic Diseases;2004-02-01

4. Scleroderma epidemiology;Rheumatic Disease Clinics of North America;2003-05

5. A case-control study on risk factors for scleroderma;Japanese Journal of Rheumatology;1998-09
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