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New case of contiguous gene syndrome at chromosome 8p11.2p12CAU, M; CONGIU, R; ORIGA, R et al.American journal of medical genetics. 2005, Vol 136A, Num 2, pp 221-222, issn 0148-7299, 2 p.Article

Identification of a novel T-insertion polymorphism at the DMD locusMUNTONI, F; CAU, M; CONGIU, R et al.Human genetics. 1993, Vol 92, Num 1, issn 0340-6717, p. 103Article

Mesangiolysis and endothelial lesions due to peroxidative damage in rabbitsSTRATTA, P; CANAVESE, C; FERRERO, T et al.Nephron. 1989, Vol 51, Num 2, pp 250-256, issn 0028-2766Article

Diagnosis of DMD carrier status in a family with No known affected malesMUNTONI, F; MATEDDU, A; CAU, M et al.Developmental medicine and child neurology (Print). 1993, Vol 35, Num 1, pp 70-73, issn 0012-1622Article

Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrierMUNTONI, F; MATEDDU, A; MARROSU, M. G et al.Clinical genetics. 1992, Vol 42, Num 1, pp 35-38, issn 0009-9163Article

Brief report : deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathyMUNTONI, F; CAU, M; MELIS, M. A et al.The New England journal of medicine. 1993, Vol 329, Num 13, pp 921-925, issn 0028-4793Article

Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyMUNTONI, F; MATEDDU, A; CIANCHETTI, C et al.Journal of neurology, neurosurgery and psychiatry. 1993, Vol 56, Num 1, pp 26-31, issn 0022-3050Article

Germinal mosaicism in a Duchenne muscular dystrophy family : implications for genetic counsellingMELIS, M. A; CAU, M; CONGIU, R et al.Clinical genetics. 1993, Vol 43, Num 5, pp 247-249, issn 0009-9163Article

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