G6PD Aures: a new mutation (48 lle → Thr) causing mild G6PD deficiency is associated with favism von Nafa, Khedoudja, Reghis, Abderrezak, Osmani, Naima, Baghli, Lamia, Benabadji, Mohamed, Kaplan, Jean-Claude, Vulliamy, Thomas J., Luzzatto, Lucio

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Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X von Chafa, Ouerdia, Tagzirt, Madjid, Tapon-Bretaudière, Jacqueline, Reghis, Abderrezak, Fischer, Anne-Marie, LeBonniec, Bernard F

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Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis von Borensztajn, Keren, Chafa, Ouerdia, Alhenc‐Gelas, Martine, Salha, Siham, Reghis, Abderrezak, Fischer, Anne‐Marie, Tapon‐Bretaudière, Jacqueline

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Recurrence of a Phe31Ser mutation in the Gla domain of blood coagulation factor X, in unrelated Algerian families: a founder effect? von Akhavan, Sepideh, Chafa, Ouerdia, Nsoure Obame, Fatou, Torchet, Marie-Françoise, Reghis, Abderrezak, Fischer, Anne-Marie, Tapon-Bretaudière, Jacqueline

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Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain von Borensztajn, Keren, Chafa, Ouerdia, Le Bonniec, Bernard, Wajcman, Henri, Reghis, Abderrezak, Fischer, Anne-Marie, Tapon-Bretaudière, Jacqueline

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Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12 von Azlbi, Kemal, Bachner, Luclen, S.Beckmann, Jacques, Matsumura, Kllchlro, Hamouda, Elhadl, Chaouch, Mallka, Chaouch, Athmane, Alt-Ouarab, Rachlda, Vlgnal, Alaln, Welssenbach, Jean, Vinet, Marie-Claude, Leturcq, France, Collln, Huguette, M.S.Tomé, Fernando, Reghis, Abderrezak, Fardeau, Michel, P.Campbell, Kevin, Kaplan, Jean-Claude

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At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria von Nafa, K, Reghis, A, Osmani, N, Baghli, L, Aït-Abbes, H, Benabadji, M, Kaplan, J C, Vulliamy, T, Luzzatto, L

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Screening for mutations in factor VIII gene using the single-strand conformation polymorphism von Nafa, Khédoudja, Meriane, Farida, Chellali, Thouraya, Benabadji, Mohamed, Reghis, Abderrezak, Viemont, Michèle, Kaplan, Jean-Claude, Delpech, Marc

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Endogenous Proteolysis of Membrane-Bound Red Cell Cytochrome-b5 Reductase in Adults and Newborns: Its Possible Relevance to the Generation of the Soluble “Methemoglobin Reductase”... von Choury, Danièle, Reghis, Abderrezak, Pichard, Anne-Lise, Kaplan, Jean-Claude

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