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The British Journal of Dermatology|April 1, 1979
Characterization of dermal collagen in systemic sclerosisC R Lovell, A C Nicholls, V C Duance, et al.
Clinical Genetics|February 1, 1997
Congenital cutis laxa and lysyl oxidase deficiencyA Khakoo, R Thomas, R Trompeter, et al.
The British Journal of Dermatology|August 1, 1991
Platelet and coagulation studies in Ehlers-Danlos syndromeA Anstey, K Mayne, M Winter, et al.
Stroke|April 1, 1990
Cerebrovascular disease in Ehlers-Danlos syndrome type IVW I Schievink, M Limburg, J W Oorthuys, et al.
American Journal of Human Genetics|September 1, 1992
Substitution of aspartate for glycine 1018 in the type III procollagen (COL3A1) gene causes type IV Ehlers-Danlos syndrome: the mutated allele is present in most blood leukocytes of the asymptomatic and mosaic motherS Kontusaari, G Tromp, H Kuivaniemi, et al.
Clinical and Experimental Dermatology|May 16, 2013
Palmoplantar contractures in childhood: a rare complication of vascular Ehlers-Danlos syndromeA C Foulkes, R Pollitt, G Sobey, et al.
Nucleic Acids Research|July 11, 1985
A highly polymorphic region 3' to the human type II collagen geneN G Stoker, K S Cheah, J R Griffin, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 1994
Fibrillin secretion and microfibril assembly by Marfan dermal fibroblastsC M Kielty, J E Phillips, A H Child, et al.
Human Mutation|January 1, 1995
Efficient strategy for the detection of mutations in acrogeric Ehlers-Danlos syndrome type IVP H Johnson, A J Richards, J C Lloyd, et al.
Clinical and Experimental Dermatology|September 1, 1991
Lipoid proteinosis--new immunopathological observationsJ A Newton, S Rasbridge, A Temple, et al.
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