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Connective Tissue Research|January 1, 1993
An intronic deletion leading to skipping of exon 21 of COL1A2 in a boy with mild osteogenesis imperfectaA Superti-Furga, M Raghunath, F M Pistone, et al.Pediatric Research|October 1, 1994
Prenatal diagnosis of collagen disorders by direct biochemical analysis of chorionic villus biopsiesM Raghunath, B Steinmann, C Delozier-Blanchet, et al.American Journal of Medical Genetics|May 7, 2002
Homozygous Gly530Ser substitution in COL5A1 causes mild classical Ehlers-Danlos syndromeC Giunta, L Nuytinck, M Raghunath, et al.The Biochemical Journal|September 15, 1994
Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndromeM Raghunath, C M Kielty, K Kainulainen, et al.Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1998
Ehlers-Danlos Syndrome Type VI (EDS VI): problems of diagnosis and managementP Heim, M Raghunath, L Meiss, et al.The Journal of Investigative Dermatology|May 1, 1996
Fibrillin and elastin expression in skin regenerating from cultured keratinocyte autografts: morphogenesis of microfibrils begins at the dermo-epidermal junction and precedes elastic fiber formationM Raghunath, T Bächi, M Meuli, et al.The Journal of Clinical Investigation|September 1, 1996
Cross-linking of the dermo-epidermal junction of skin regenerating from keratinocyte autografts. Anchoring fibrils are a target for tissue transglutaminaseM Raghunath, B Höpfner, D Aeschlimann, et al.Pageof 23