Authors: Granel, B Serratrice, J Bouabdallah, R Pache, X Weiller-Merli, C Swiader, L Aquaron, R Disdier, P Nordmann, Y Weiller, PJ

Citation: B. Granel et al., Atypical porphyria cutanea tarda in a patient with chronic myelogenous leukemia, DERMATOLOGY, 203(1), 2001, pp. 82-83

Authors: Robreau-Fraolini, AM Puy, H Aquaron, C Bogard, C Traore, M Nordmann, Y Aquaron, R Deybach, JC

Citation: Am. Robreau-fraolini et al., Porphobilinogen deaminase gene in African and Afro-Caribbean ethnic groups: mutations causing acute intermittent porphyria and specific intragenic polymorphisms, HUM GENET, 107(2), 2000, pp. 150-159

Authors: Granel, B Serratrice, J Bouabdallah, R Pache, X Weiller-Merli, C Swiader, L Aquaron, R Disdier, P Nordmann, Y Weiller, PJ

Citation: B. Granel et al., Chronic myeloid leukemia, REV MED IN, 21, 2000, pp. 410S-411S

Authors: Aquaron, R

Citation: R. Aquaron, Tradition of basic and applied pigment cell research in Marseilles, CELL MOL B, 45(7), 1999, pp. 877-882

Authors: Aquaron, R

Citation: R. Aquaron, 8th Meeting of the European Society for Pigment Cell Research - September 23-26, 1998 - Prague, Czech Republic - Foreword, CELL MOL B, 45(7), 1999, pp. V-V

Authors: de Bernabe, DBV Jimenez, FJ Aquaron, R de Cordoba, SR

Citation: Dbv. De Bernabe et al., Analysis of alkaptonuria (AKU) mutations and polymorphisms reveals that the CCC sequence motif is a mutational hot spot in the homogentisate 1,2 dioxygenase gene (HGO), AM J HU GEN, 64(5), 1999, pp. 1316-1322