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The British Journal of Dermatology|July 1, 1987
Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type IIIA De Paepe, A Nicholls, P Narcisi, et al.
The British Journal of Ophthalmology|March 24, 2000
COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromesA J Richards, S Martin, J R Yates, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|October 1, 1992
Ehlers Danlos syndrome type I with novel dental featuresF M Pope, A Komorowska, K W Lee, et al.
American Journal of Human Genetics|February 1, 1990
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2B Sykes, D Ogilvie, P Wordsworth, et al.
The British Journal of Ophthalmology|May 1, 1981
Angioid streaks in Jamaican patients with homozygous sickle cell diseaseA M Hamilton, F M Pope, P I Condon, et al.
Eye (London, England)|January 1, 1994
Stickler syndrome: correlation between vitreoretinal phenotypes and linkage to COL 2A1M P Snead, S J Payne, D E Barton, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
The British Journal of Dermatology|May 30, 2019
Electron microscopy in the diagnosis of Ehlers-Danlos syndromes: correlation with clinical and genetic investigationsC Angwin, N Ghali, D Baker, et al.
Journal of Medical Genetics|February 1, 1990
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11J de Groote, P A Farndon, M V Kilpatrick, et al.
Journal of Medical Genetics|October 1, 1994
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalitiesM G Dunnill, A J Richards, G Milana, et al.
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