MOLECULAR GENETICS OF HEARING LOSS von Petit, Christine, Levilliers, Jacqueline, Hardelin, Jean-Pierre

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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene von Denoyelle, Françoise, Weil, Dominique, Maw, Marion A., Wilcox, Stephen A., Lench, Nicholas J., Allen-Powell, Denise R., Osborn, Amelia H., Dahl, Hans-Henrik M., Middleton, Anna, Houseman, Mark J., Dodé, Catherine, Marlin, Sandrine, Boulila-ElGaïed, Amel, Grati, Mohammed, Ayadi, Hammadi, BenArab, Saïda, Bitoun, Pierre, Lina-Granade, Geneviève, Godet, Jacqueline, Mustapha, Mirna, Loiselet, Jacques, El-Zir, Élie, Aubois, Anne, Joannard, Alain, Levilliers, Jacqueline, Garabédian, Éréa-Noël, Mueller, Robert F., McKinlay Gardner, R. J., Petit, Christine

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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome von Soussi-Yanicostas, Nadia, Baverel, Françoise, Dupont, Jean-Michel, Cabrol, Sylvie, Levilliers, Jacqueline, Bouchard, Philippe, Kottler, Marie-Laure, Sanchez-Franco, Franco, Delmaghani, Sedigheh, Petit, Christine, Hardelin, Jean-Pierre, Delpech, Marc, De Paepe, Anne, Carel, Jean-Claude, Compain-Nouaille, Sylvie, Richard, Odile, Young, Jacques, Coimbra, Roney S, Goulet-Salmon, Barbara, Cruaud, Corinne, Le Tessier, Dominique, Vermeulen, Stefan, Delemarre-van de Waal, Henriette, Le Dû, Nathalie, Speleman, Frank, Saura, Robert, Bachelot, Yvan, Dodé, Catherine, Amalfitano, Andrea, Pêcheux, Christophe

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X Chromosome-Linked Kallmann Syndrome: Stop Mutations Validate the Candidate Gene von Hardelin, Jean-Pierre, Levilliers, Jacqueline, del Castillo, Ignacio, Cohen-Salmon, Martine, Legouis, Renaud, Blanchard, Stephane, Compain, Sylvie, Bouloux, Pierre, Kirk, Jeremy, Moraine, Claude, Chaussain, Jean-Louis, Weissenbach, Jean, Petit, Christine

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MUTATIONAL ANALYSIS OF SRY - NONSENSE AND MISSENSE MUTATIONS IN XY SEX REVERSAL von HAWKINS, TAYLOR, A, BERTA, P, LEVILLIERS, J, VANDERAUWERA, B, GOODFELLOW, PN

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Long-Range Restriction Map of the Terminal Part of the Short Arm of the Human X Chromosome von Petit, Christine, Levilliers, Jacqueline, Weissenbach, Jean

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Physical mapping of the human pseudo‐autosomal region; comparison with genetic linkage map von Petit, C., Levilliers, J., Weissenbach, J.

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Exchange of Terminal Portions of X- and Y-chromosomal Short Arms in Human XY Females von Levilliers, Jacqueline, Quack, Bernadette, Weissenbach, Jean, Petit, Christine

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Defective myosin VIIA gene responsible for Usher syndrome type 1B von WEIL, D, BLANCHARD, S, KELLEY, P. M, KIMBERLING, W. J, WAGENAAR, M, LEVI-ACOBAS, F, LARGET-PIET, D, MUNNICH, A, STEEL, K. P, BROWN, S. D. M, PETIT, C, KAPLAN, J, GUILFORD, P, GIBSON, F, WALSH, J, MBURU, P, VARELA, A, LEVILLIERS, J, WESTON, M. D

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A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy von Franco, Brunella, Meroni, Germana, Parenti, Giancarlo, Levilliers, Jacqueline, Bernard, Loris, Gebbia, Marinella, Cox, Liza, Maroteaux, Pierre, Sheffield, Leslie, Rappold, Gudrun A, Andria, Generoso, Petit, Christine, Ballabio, Andrea

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Tissue-Specific Expression of the Rat Albumin Gene: Genetic Control of Its Extinction in Microcell Hybrids von Petit, Christine, Levilliers, Jacqueline, Ott, Marie-Odile, Weiss, Mary C.

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DFNA3 von Denoyelle, F., Weil, D., Levilliers, J., Petit, C.

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A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q von Weissenbach, Jean, Arab, Saida Ben, Belkahia, Ali, Guilford, Parry, Blanchard, Stéphane, Levilliers, Jacqueline, Petit, Christine

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Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner von Soussi-Yanicostas, N, Faivre-Sarrailh, C, Hardelin, J P, Levilliers, J, Rougon, G, Petit, C

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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules von Legouis, Renaud, Hardelin, Jean-Pierre, Levilliers, Jacqueline, Claverie, Jean-Michel, Compain, Sylvia, Wunderle, Véronique, Millasseau, Philippe, Le Paslier, Denis, Cohen, Daniel, Caterina, Dominique, Bougueleret, Lydie, Delemarre-Van de Waal, Henriette, Lutfalla, Georges, Weissenbach, Jean, Petit, Christine

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Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3 : close linkage to the hypervariable repeat sequence CRI-S232 von MEITINGER, T, HEYE, B, PETIT, C, LEVILLIERS, J, GOLLA, A, MORAINE, C, DALLA PICCOLA, B, SIPPELL, W. G, MURKEN, J, BALLABIO, A

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Kallmann Syndrome von Hardelin, J.-P., Soussi-Yanicostas, N., Ardouin, O., Levilliers, J., Petit, C.

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Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome von Hardelin, Jean-Pierre, Levilliers, Jacqueline, Blanchard, Stéphane, Carel, Jean-Claude, Leutenegger, Marc, Pinard-Bertelletto, Jean-Pierre, Bouloux, Pierre, Petit, Christine

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Characterization and Chromosomal Assignment of a Human cDNA Encoding a Protein Related to the Murine 102-kDa Cadherin-Associated Protein (α-Catenin) von Claverie, Jean-Michel, Hardelin, Jean-Pierre, Legouis, Renaud, Levilliers, Jacqueline, Bougeuleret, Lydie, Mattei, Marie-Geneviève, Petit, Christine

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Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system von Soussi-Yanicostas, N, Hardelin, J P, Arroyo-Jimenez, M M, Ardouin, O, Legouis, R, Levilliers, J, Traincard, F, Betton, J M, Cabanié, L, Petit, C

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