RMND1 mutations in two siblings: Severe renal hypoplasia but different levels of extrarenal abnormality severity: The ethics of decision making von Broenen, E., Ranchin, B., Besmond, C., Freychet, C., Fouilhoux, A., Perouse de Montclos, T., Ville, D., Bacchetta, J.

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Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study von Gabolde, M, Guilloud-Bataille, M, Feingold, J, Besmond, C

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The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis von Gabolde, M, Hubert, D, Guilloud-Bataille, M, Lenaerts, C, Feingold, J, Besmond, C

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Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes von Guilmeau, S, Niot, I, Laigneau, J P, Devaud, H, Petit, V, Brousse, N, Bouvier, R, Ferkdadji, L, Besmond, C, Aggerbeck, L P, Bado, A, Samson-Bouma, M E

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Apports de la génétique au diagnostic des troubles du spectre autistique von Demily, C., Assouline, M., Boddaert, N., Barcia, G., Besmond, C., Poisson, A., Sanlaville, D., Munnich, A.

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Polymorphisms of the Receptor of Advanced Glycation Endproducts (RAGE) and the development of nephropathy in type 1 diabetic patients von Prevost, G, Fajardy, I, Besmond, C, Balkau, B, Tichet, J, Fontaine, P, Danze, PM, Marre, M

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Microsatellite polymorphism in the promoter sequence of the elongation factor 3 gene of Candida albicans as the basis for a typing system von BRETAGNE, S, COSTA, J.-M, BESMOND, C, CARSIQUE, R, CALDERONE, R

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Preparing and Using M13‐Derived Vectors von Greenstein, David, Besmond, Claude

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Potential of denaturing gradient gel electrophoresis for scanning of β‐thalassemia mutations in India von Gorakshakar, A.C., Pawar, A.R., Nadkarni, A.H., Lu, C.Y., Mohanty, D., Krishnamoorthy, R., Besmond, C., Colah, R.B.

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Evaluation of Parental Mitochondrial Inheritance in Neonates Born after Intracytoplasmic Sperm Injection von Danan, Claude, Sternberg, Damien, Van Steirteghem, André, Cazeneuve, Cécile, Duquesnoy, Philippe, Besmond, Claude, Goossens, Michel, Lissens, Willy, Amselem, Serge

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Exclusion of WNT4 as a major gene in Rokitansky-Küster-Hauser anomaly von Clément-Ziza, Mathieu, Khen, Naziha, Gonzales, Jacques, Crétolle-Vastel, Célia, Picard, Jean-Yves, Tullio-Pelet, Anna, Besmond, Claude, Munnich, Arnold, Lyonnet, Stanislas, Nihoul-Fékété, Claire

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Molecular characterization of cystic fibrosis: 16 Novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and... von Fanen, Pascale, Ghanem, Nada, Vidaud, Michel, Besmond, Claude, Martin, Josiane, Costes, Bruno, Plassa, Francois, Goossens, Michel

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Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two families von Desbois-Mouthon, C., Girodon, E., Ghanem, N., Caron, M., Pennerath, A., Conteville, P., Magre, J., Besmond, C., Goossens, M., Capeau, J., Amselem, S.

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Characterization of a putative type IV aminophospholipid transporter P-type ATPase von Flamant, Stéphane, Pescher, Pascale, Lemercier, Brigitte, Clément-Ziza, Mathieu, Képès, Franois, Fellous, Marc, Milon, Geneviève, Marchal, Gilles, Besmond, Claude

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GeneRetriever: software to extract all genes and transcripts in between two genetic markers to assist design of human custom microarrays von Clément-Ziza, Mathieu, Brody, Yehuda, Munnich, Arnold, Lyonnet, Stanislas, Besmond, Claude

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Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma von Blanquet, Véronique, Turleau, Catherine, Gross-Morand, Marie Sylvie, Sénamaud-Beaufort, Catherine, Doz, François, Besmond, Claude

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Enhanced cloning efficiency of mouse bone marrow macrophage progenitors correlates with increased content of CSF-1 receptor of their progeny at low oxygen tension von Flamant, Stéphane, Lebastard, Maï, Pescher, Pascale, Besmond, Claude, Milon, Geneviève, Marchal, Gilles

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Molecular cloning of cDNA for rat L-type pyruvate kinase and aldolase B von Simon, M P, Besmond, C, Cottreau, D, Weber, A, Chaumet-Riffaud, P, Dreyfus, J C, Trépat, J S, Marie, J, Kahn, A

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A Simple Approach to the Characterization of Three Common Indian β-Thalassemia Mutations by Artificially Created Restriction Sites von Pawar, A. R., Lu, C. Y., Besmond, C., Gorakshakar, A. C., Colah, R. B., Mohanty, D., Krishnamoorthy, R.

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Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes von Guilmeau, Sandra, Niot, I., Laigneau, J., Devaud, H., Petit, V., Brousse, N., Bouvier, R., Ferkdadji, L., Besmond, C., Aggerbeck, L., Bado, A., Samson-Bouma, M.

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