Arthrochalasis Type of Ehlers–Danlos Syndrome (EDS Types VIIA and VIIB) and Related Disorders-Reference-Cited by-同舟云学术

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Arthrochalasis Type of Ehlers–Danlos Syndrome (EDS Types VIIA and VIIB) and Related Disorders

Published:2014 Issue: Volume: Page:217-228
ISSN:
Container-title:Osteogenesis Imperfecta
language:
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Author:

Giunta Cecilia,Steinmann Beat

Publisher

Elsevier

Reference52 articles.

1. Ehlers–Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers–Danlos National Foundation (USA) and Ehlers–Danlos Support Group (UK);Beighton;Am J Med Genet,1998

2. The Ehlers–Danlos syndrome. Connective tissue and its heritable disorders;Steinmann,2002

3. Arthrochalasis multiplex congenita; congenital flaccidity of the joints;Hass;J Bone Joint Surg Am,1958

4. Procollagen peptidase deficiency in a form of the Ehlers–Danlos syndrome;Lichtenstein;Trans Assoc Am Physicians,1973

5. Defect in conversion of procollagen to collagen in a form of Ehlers–Danlos syndrome;Lichtenstein;Science,1973

Cited by 2 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. Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome;American Journal of Medical Genetics Part A;2020-02-24

2. The Ehlers-Danlos syndromes, rare types;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2017-03

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