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Page 1
Mutational analysis of the OA1 gene in ocular albinism.
Camand O, Boutboul S, Arbogast L, Roche O, Sternberg C, Sutherland J, Levin A, Héon E, Menasche M, Dufier J, Abitbol M. Camand O, et al. Among authors: sternberg c. Ophthalmic Genet. 2003 Sep;24(3):167-73. doi: 10.1076/opge.24.3.167.15605. Ophthalmic Genet. 2003. PMID: 12868035
Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy.
Marchant D, Gogat K, Dureau P, Sainton K, Sternberg C, Gadin S, Dollfus H, Brasseur G, Hache JC, Dumur V, Puech V, Munier F, Schorderet DF, Marsac C, Menasche M, Dufier JL, Abitbol M. Marchant D, et al. Among authors: sternberg c. Ophthalmic Genet. 2002 Sep;23(3):167-74. doi: 10.1076/opge.23.3.167.7880. Ophthalmic Genet. 2002. PMID: 12324875
Behçet syndrome associated with protein S deficiency.
Chafa O, Fischer AM, Meriane F, Chellali T, Sternberg C, Otmani F, Benabadji M. Chafa O, et al. Among authors: sternberg c. Thromb Haemost. 1992 Jan 23;67(1):1-3. Thromb Haemost. 1992. PMID: 1535461
A new case of 'type II' inherited protein S deficiency.
Chafa O, Fischer AM, Meriane F, Chellali F, Rahal S, Sternberg C, Benabadji M. Chafa O, et al. Among authors: sternberg c. Br J Haematol. 1989 Dec;73(4):501-5. doi: 10.1111/j.1365-2141.1989.tb00288.x. Br J Haematol. 1989. PMID: 2532929
Antithrombin III Alger: a new homozygous AT III variant.
Fischer AM, Cornu P, Sternberg C, Mériane F, Dautzenberg MD, Chafa O, Beguin S, Desnos M. Fischer AM, et al. Among authors: sternberg c. Thromb Haemost. 1986 Apr 30;55(2):218-21. Thromb Haemost. 1986. PMID: 3715788
660 results