Shockwave lithotripsy of salivary duct stones by Iro, H., Fodra, C., Waitz, G., Nitsche, N., Heinritz, H.H., Schneider, H.Th, Benninger, J., Ell, Ch

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Prevalence of abnormal mucosal findings in patients in HNO practices by Löhler, J, Gerstner, A O H, Bootz, F, Heinritz, H, Fryen, A, Fryen, G, Holstein, N, Lingg, A, Kleeberg, J, Langhoff, W, Rösch, G, Hanisch, A, Schneeberg, E, Heinrich, D, Walther, L E

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Prävalenz auffälliger Schleimhautbefunde bei Patienten in HNO-Praxen by Löhler, J., Gerstner, A.O.H., Bootz, F., Heinritz, H., Fryen, A., Fryen, G., Holstein, N., Lingg, A., Kleeberg, J., Langhoff, W., Rösch, G., Hanisch, A., Schneeberg, E., Heinrich, D., Walther, L.E.

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Longitudinal Phenotypes of Respiratory Health in a High-Risk Urban Birth Cohort by Bacharier, Leonard B, Beigelman, Avraham, Calatroni, Agustin, Jackson, Daniel J, Gergen, Peter J, O'Connor, George T, Kattan, Meyer, Wood, Robert A, Sandel, Megan T, Lynch, Susan V, Fujimura, Kei E, Fadrosh, Douglas W, Santee, Clark A, Boushey, Homer, Visness, Cynthia M, Gern, James E

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Tiny Earth: A Big Idea for STEM Education and Antibiotic Discovery by Hurley, Amanda, Chevrette, Marc G, Acharya, Deepa D, Lozano, Gabriel L, Garavito, Manuel, Heinritz, Jen, Balderrama, Luis, Beebe, Mara, DenHartog, Martel L, Corinaldi, Kamiyah, Engels, Renee, Gutierrez, Alyssa, Jona, Orli, Putnam, Josephine H I, Rhodes, Brody, Tsang, Tiffany, Hernandez, Simon, Bascom-Slack, Carol, Blum, Jessamina E, Price, Paul A, Davis, Debra, Klein, Joanna, Pultorak, Joshua, Sullivan, Nora L, Mouncey, Nigel J, Dorrestein, Pieter C, Miller, Sarah, Broderick, Nichole A, Handelsman, Jo

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Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers by Antoniou, Antonis C, Soucy, Penny, McGuffog, Lesley, Healey, Sue, Lee, Andrew, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Barile, Monica, Pasini, Barbara, Dolcetti, Riccardo, Giannini, Giuseppe, Varesco, Liliana, Radice, Paolo, Greene, Mark H., Glendon, Gord, Birk Jensen, Uffe, Crüger, Dorthe G., Caligo, Maria A., Laitman, Yael, Milgrom, Roni, Kaufman, Bella, Friedman, Eitan, Lindblom, Annika, Ehrencrona, Hans, Nathanson, Katherine L., Domchek, Susan M., Rebbeck, Timothy, Jakubowska, Ania, Gronwald, Jacek, Byrski, Tomasz, Cybulski, Cezary, Osorio, Ana, Ramón y Cajal, Teresa, Fostira, Florentia, Hogervorst, Frans B., Hooning, Maartje J., Meijers-Heijboer, Hanne E.J., Gómez Garcia, Encarna B., Peock, Susan, Platte, Radka, Lalloo, Fiona, Eeles, Ros, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-ren, Cook, Jackie, Douglas, Fiona, Paterson, Joan, John Kennedy, M., Miedzybrodzka, Zosia, Godwin, Andrew, Stoppa-Lyonnet, Dominique, Buecher, Bruno, Tirapo, Carole, Barjhoux, Laure, Faivre, Laurence, Nogues, Catherine, Rouleau, Etienne, Pujol, Pascal, Coupier, Isabelle, Frénay, Marc, Daly, Mary B., John, Esther M., Singer, Christian F., Catharina Dressler, Anne, Offit, Kenneth, Rodriguez, Gustavo, Small, Laurie, Boggess, John, Blank, Stephanie, Basil, Jack, Ewart Toland, Amanda, Montagna, Marco, Tognazzo, Silvia, Blanco, Ignacio, Pharoah, Paul D.P., Karlan, Beth Y., Walsh, Christine S., Olah, Edith, Teo, Soo-Hwang, Beattie, Mary S., van Rensburg, Elizabeth J., Sluiter, Michelle D., Diez, Orland, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Varon-Mateeva, Raymonda, Niederacher, Dieter, Arnold, Norbert, Gadzicki, Dorothea, Caldes, Trinidad, de la Hoya, Miguel, Chen, Xiaoqing, Spurdle, Amanda B., Fredericksen, Zachary, Couch, Fergus, Simard, Jacques

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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... by 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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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 by 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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Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl by Teich, Niels, Nemoda, Zsófia, Köhler, Henrik, Heinritz, Wolfram, Mössner, Joachim, Keim, Volker, Sahin-Tóth, Miklós

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Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome by 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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Pre-eclampsia as a ‘Three Stage Problem’—A Workshop Report by Stepan, H, Faber, R, Froster, U.G, Heinritz, W, Wallaschofski, H, Dechend, R, Walther, T, Huppertz, B

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Population statistics in Cyprus: in the mist of statistics by Brey, H, Heinritz, G

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Molekulargenetischer Mutationsnachweis im PTPN11-Gen beim Multiple-Lentigines- (LEOPARD-)Syndrom by Froster, U. G., Glander, H.-J., Heinritz, W.

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Methods in retail geography. Special Issue by HEINRITZ, G, REYNOLDS, J, BORGERS, A, TIMMERMANS, H, TERASAKA, A, BORCHERT, J.G, GUY, C.M, LÖFFLER, G, MONHEIM, R, CLARKE, G, HERNANDEZ, T, BENNISON, D, CORNELIUS, S, VAN DER WAERDEN, P

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Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome by Froster, U G, Glander, H-J, Heinritz, W

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REGIONALBEWUSSTSEIN“. ZUM STAND DER DISKUSSION UM EINEN STEIN DES ANSTOSSES by BLOTEVOGEL, HANS H., HEINRITZ, GÜNTER, POPP, HERBERT

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Bevölkerungsbewegungen in Zypern im Nebel der Statistik by BREY, H, HEINRITZ, G

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Molekulargenetischer Mutationsnachweis im PTRN11-Gen beim Multiple-Lentigines-(LEOPARD-)Syndrom by G.FROSTER, U, GLANDER, H.-J, HEINRITZ, W

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Regionalbewusstein. Zum Stand der Diskussion um einen Stein des Anstolsses/Regional Consciousness-On Recent Discussions about a Controversial Issue by Blotevogel, H H, Heinritz, G, Popp, H

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Regionalbewusstsein . Zum Stand der Diskussion um einen Stein des Anstosses Conscience régionale . Etat de la discussion autour de la cause du scandale by BLOTEVOGEL, H. H, HEINRITZ, G, POPP, H

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