Mutation in Na v 1.7 causes high olfactory sensitivity von Haehner, A, Hummel, T, Heinritz, W, Krueger, S, Meinhardt, M, Whitcroft, K L, Sabatowski, R, Gossrau, G

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Cysteine-sparing notch3 mutations: Cadasil or cadasil variants? von SCHEID, R, HEINRITZ, W, LEYHE, T, THAI, D. R, SCHOBER, R, STRENGE, S, VON CRAMON, D. Y, FROSTER, U. G

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Multiple trichoepitheliomas - a novel mutation in the CYLD gene von Amaro, C, Freitas, I, Lamarão, P, Afonso, A, Skrzypczak, M, Heinritz, W

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TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings von Gruenauer-Kloevekorn, C, Clausen, I, Weidle, E, Wolter-Roessler, M, Tost, F, Völcker, H E, Schulze, D P, Heinritz, W, Reinhard, T, Froster, U, Duncker, G, Schorderet, D, Auw-Haedrich, C

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Vascular parkinsonism in a CADASIL case with an intact nigrostriatal dopaminergic system von Wegner, F, Strecker, K, Schwarz, J, Wagner, A, Heinritz, W, Sommerer, F, Thal, D R, Schneider, J-P, Kendziorra, K, Sabri, O

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Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome von Heinritz, W, Moschik, A, Kujat, A, Spranger, S, Heilbronner, H, Demuth, S, Bier, A, Tihanyi, M, Mundlos, S, Gruenauer-Kloevekorn, C, Froster, U G

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A new mutation in the GJB3 gene in a patient with erythrokeratodermia variabilis von Renner, R, Paasch, U, Simon, JC, Froster, UG, Heinritz, W

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Evidence for a Founder Effect of the Germline Fumarate Hydratase Gene Mutation R58P causing Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) von Heinritz, W., Paasch, U., Sticherling, M., Wittekind, C., Simon, J.C., Froster, U.G., Renner, R.

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Transcriptional regulator PRDM12 is essential for human pain perception von Chen, Ya-Chun, Auer-Grumbach, Michaela, Matsukawa, Shinya, Zitzelsberger, Manuela, Themistocleous, Andreas C, Strom, Tim M, Samara, Chrysanthi, Moore, Adrian W, Cho, Lily Ting-Yin, Young, Gareth T, Weiss, Caecilia, Schabhüttl, Maria, Stucka, Rolf, Schmid, Annina B, Parman, Yesim, Graul-Neumann, Luitgard, Heinritz, Wolfram, Passarge, Eberhard, Watson, Rosemarie M, Hertz, Jens Michael, Moog, Ute, Baumgartner, Manuela, Valente, Enza Maria, Pereira, Diego, Restrepo, Carlos M, Katona, Istvan, Dusl, Marina, Stendel, Claudia, Wieland, Thomas, Stafford, Fay, Reimann, Frank, von Au, Katja, Finke, Christian, Willems, Patrick J, Nahorski, Michael S, Shaikh, Samiha S, Carvalho, Ofélia P, Nicholas, Adeline K, Karbani, Gulshan, McAleer, Maeve A, Cilio, Maria Roberta, McHugh, John C, Murphy, Sinead M, Irvine, Alan D, Jensen, Uffe Birk, Windhager, Reinhard, Weis, Joachim, Bergmann, Carsten, Rautenstrauss, Bernd, Baets, Jonathan, De Jonghe, Peter, Reilly, Mary M, Kropatsch, Regina, Kurth, Ingo, Chrast, Roman, Michiue, Tatsuo, Bennett, David L H, Woods, C Geoffrey, Senderek, Jan

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A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene von Heinritz, W., Grunewald, S., Strenge, S., Schütz, A., Froster, U.G., Glander, H.J., Paasch, U., Simon, J.C.

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Mutation in Nav1.7 causes high olfactory sensitivity von Haehner, A., Hummel, T., Heinritz, W., Krueger, S., Meinhardt, M., Whitcroft, K. L., Sabatowski, R., Gossrau, G.

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Pre-eclampsia as a ‘Three Stage Problem’—A Workshop Report von Stepan, H, Faber, R, Froster, U.G, Heinritz, W, Wallaschofski, H, Dechend, R, Walther, T, Huppertz, B

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Another case of autosomal dominant exstrophy of the bladder von Froster, U. G., Heinritz, W., Bennek, J., Horn, L. C., Faber, R.

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Detection of five new mutations in the APC gene using denaturing high-performance liquid chromatography von Heinritz, W, Kujat, A, Froster, UG

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Mutation in Nav 1.7 causes high olfactory sensitivity von Haehner, A, Hummel, T, Heinritz, W, Krueger, S, Meinhardt, M, Whitcroft, K L, Sabatowski, R, Gossrau, G

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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of B... von Mulligan, Anna Marie, Couch, Fergus J, Barrowdale, Daniel, Domchek, Susan M, Eccles, Diana, Nevanlinna, Heli, Ramus, Susan J, Robson, Mark, Sherman, Mark, Spurdle, Amanda B, Wappenschmidt, Barbara, Lee, Andrew, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M, Janavicius, Ramunas, Hansen, Thomas vO, Nielsen, Finn C, Ejlertsen, Bent, Osorio, Ana, Muñoz-Repeto, Iván, Durán, Mercedes, Godino, Javier, Pertesi, Maroulio, Benítez, Javier, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Cattaneo, Elisa, Bonanni, Bernardo, Viel, Alessandra, Pasini, Barbara, Papi, Laura, Ottini, Laura, Savarese, Antonella, Bernard, Loris, Radice, Paolo, Hamann, Ute, Verheus, Martijn, Meijers-Heijboer, Hanne E J, Wijnen, Juul, Gómez García, Encarna B, Nelen, Marcel R, Kets, C Marleen, Seynaeve, Caroline, Tilanus-Linthorst, Madeleine M A, van der Luijt, Rob B, van Os, Theo, Rookus, Matti, Frost, Debra, Jones, J Louise, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Donaldson, Alan, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, Barwell, Julian, Side, Lucy E, McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew K, Schmutzler, Rita K, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Fiebig, Britta, Heinritz, Wolfram, Schäfer, Dieter, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Fassy-Colcombet, Marion, Cornelis, François, Mazoyer, Sylvie, Léoné, Mélanie, Boutry-Kryza, Nadia, Hardouin, Agnès, Berthet, Pascaline, Muller, Danièle, Fricker, Jean-Pierre, Mortemousque, Isabelle, Pujol, Pascal

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Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception von Chen, Ya-Chun, Auer-Grumbach, Michaela, Matsukawa, Shinya, Zitzelsberger, Manuela, Themistocleous, Andreas C, Strom, Tim M, Samara, Chrysanthi, Moore, Adrian W, Cho, Lily Ting-Yin, Young, Gareth T, Weiss, Caecilia, Schabhüttl, Maria, Stucka, Rolf, Schmid, Annina B, Parman, Yesim, Graul-Neumann, Luitgard, Heinritz, Wolfram, Passarge, Eberhard, Watson, Rosemarie M, Hertz, Jens Michael, Moog, Ute, Baumgartner, Manuela, Valente, Enza Maria, Pereira, Diego, Restrepo, Carlos M, Katona, Istvan, Dusl, Marina, Stendel, Claudia, Wieland, Thomas, Stafford, Fay, Reimann, Frank, von Au, Katja, Finke, Christian, Willems, Patrick J, Nahorski, Michael S, Shaikh, Samiha S, Carvalho, Ofélia P, Nicholas, Adeline K, Karbani, Gulshan, McAleer, Maeve A, Cilio, Maria Roberta, McHugh, John C, Murphy, Sinead M, Irvine, Alan D, Jensen, Uffe Birk, Windhager, Reinhard, Weis, Joachim, Bergmann, Carsten, Rautenstrauss, Bernd, Baets, Jonathan, De Jonghe, Peter, Reilly, Mary M, Kropatsch, Regina, Kurth, Ingo, Chrast, Roman, Michiue, Tatsuo, Bennett, David L H, Woods, C Geoffrey, Senderek, Jan

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Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy von Grünauer-Kloevekorn, C, Braeutigam, S, Weidle, E, Wolter-Roessler, M, Tost, F, Auw-Haedrich, C, Völcker, H E, Heinritz, W, Froster, U, Duncker, G

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Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers von COUCH, Fergus J, GAUDET, Mia M, MCGUFFOG, Lesley, BARROWDALE, Daniel, LEE, Andrew, HEALEY, Sue, SINILNIKOVA, Olga M, ANDRULIS, Irene L, OZCELIK, Hilmi, MULLIGAN, Anna Marie, THOMASSEN, Mads, GERDES, Anne-Marie, ANTONIOU, Antonis C, BIRK JENSEN, Uffe, SKYTTE, Anne-Bine, KRUSE, Torben A, CALIGO, Maria A, VON WACHENFELDT, Anna, BARBANY-BUSTINZA, Gisela, LOMAN, Niklas, SOLLER, Maria, EHRENCRONA, Hans, KARLSSON, Per, RAMUS, Susan J, NATHANSON, Katherine L, REBBECK, Timothy R, DOMCHEK, Susan M, JAKUBOWSKA, Ania, LUBINSKI, Jan, JAWORSKA, Katarzyna, DURDA, Katarzyna, ZLOWOCKA, Elzbieta, HUZARSKI, Tomasz, BYRSKI, Tomasz, KUCHENBAECKER, Karoline B, GRONWALD, Jacek, CYBULSKI, Cezary, GORSKI, Bohdan, OSORIO, Ana, DURAN, Mercedes, ISABEL TEJADA, Maria, BENITEZ, Javier, HAMANN, Ute, HOGERVORST, Frans B. L, OS, Theo A. Van, SOUCY, Penny, LEEUWEN, Flora E. Van, MEIJERS-HEIJBOER, Hanne E. J, WIJNEN, Juul, BLOK, Marinus J, KETS, Marleen, HOONING, Maartje J, OLDENBURG, Rogier A, AUSEMS, Margreet G. E. M, PEOCK, Susan, BEESLEY, Jonathan, XIAOQING CHEN, XIANSHU WANG, KIRCHHOFF, Tomas

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Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive) von Uçar, Canan, Calýskan, Umran, Martini, Susanne, Heinritz, Wolfram

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