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Results: 1-2 |
Results: 2
Molecular genetics of pigmentary retinopathies: Identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes
Authors: Hamel, CP Griffoin, JM Bazalgette, C Lasquellec, L Duval, PA Bareil, C Beaufrere, L Bonnet, S Eliaou, C Marlhens, F Schmitt-Bernard, CF Tuffery, S Claustres, M Arnaud, B
Citation: Cp. Hamel et al., Molecular genetics of pigmentary retinopathies: Identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes, J FR OPHTAL, 23(10), 2000, pp. 985-995
A syndrome combining severe hypotrichosis and macular dystrophy: absence of mutations in TIMP genes
Authors: Raison-Peyron, N Duval, PA Barneon, G Durand, L Arnaud, B Meynadier, J Hamel, C
Citation: N. Raison-peyron et al., A syndrome combining severe hypotrichosis and macular dystrophy: absence of mutations in TIMP genes, BR J DERM, 143(4), 2000, pp. 902-904
Risultati: 1-2 |