Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European population von Becker, Rolf, Keller, Thomas, Wegner, Rolf-Dieter, Neitzel, Heidemarie, Stumm, Markus, Knoll, Ute, Stärk, Markus, Fangerau, Heiner, Bittles, Alan

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'Normal' nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspects von Becker, Rolf, Schmitz, Lothar, Kilavuz, Stefania, Stumm, Markus, Wegner, Rolf-Dieter, Bittner, Uta

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Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithms von Stumm, Markus, Entezami, Michael, Trunk, Nastasja, Beck, Martina, Löcherbach, Julia, Wegner, Rolf-Dieter, Hagen, Andreas, Becker, Rolf, Hofmann, Wera

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Design, fabrication, and low-power rf measurement of an X -band dielectric-loaded accelerating structure von Wei, Yelong, Bursali, Hikmet, Grudiev, Alexej, Freemire, Ben, Jing, Chunguang, Wegner, Rolf, Bedolla, Joel Sauza, Welsch, Carsten

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Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification von Starke, Heike, Nietzel, Angela, Weise, Anja, Heller, Anita, Mrasek, Kristin, Belitz, Britta, Kelbova, Christine, Volleth, Marianne, Albrecht, Beate, Mitulla, Beate, Trappe, Ralf, Bartels, Iris, Adolph, Sabine, Dufke, Andreas, Singer, Sylke, Stumm, Markus, Wegner, Rolf-Dieter, Seidel, Jörg, Schmidt, Angela, Kuechler, Alma, Schreyer, Isolde, Claussen, Uwe, von Eggeling, Ferdinand, Liehr, Thomas

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Design, fabrication, and high-gradient testing of an X -band, traveling-wave accelerating structure milled from copper halves von Argyropoulos, Theodoros, Catalan-Lasheras, Nuria, Grudiev, Alexej, Mcmonagle, Gerard, Rodriguez-Castro, Enrique, Syrachev, Igor, Wegner, Rolf, Woolley, Ben, Wuensch, Walter, Zha, Hao, Dolgashev, Valery, Bowden, Gorden, Haase, Andrew, Lucas, Thomas Geoffrey, Volpi, Matteo, Esperante-Pereira, Daniel, Rajamäki, Robin

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Characterization of ATM Gene Mutations in 66 Ataxia Telangiectasia Families von Sandoval, Natalia, Platzer, Matthias, Rosenthal, André, Dörk, Thilo, Bendix, Regina, Skawran, Britta, Stuhrmann, Manfred, Wegner, Rolf-Dieter, Sperling, Karl, Banin, Sharon, Shiloh, Yosef, Baumer, Alessandra, Bernthaler, Ulrike, Sennefelder, Helga, Brohm, Monika, Weber, Bernhard H. F., Schindler, Detlev

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Heteromorphic variants of chromosome 9 von Kosyakova, Nadezda, Grigorian, Ani, Liehr, Thomas, Manvelyan, Marina, Simonyan, Isabella, Mkrtchyan, Hasmik, Aroutiounian, Rouben, Polityko, Anna D, Kulpanovich, Anna I, Egorova, Tatiana, Jaroshevich, Evgenia, Frolova, Alla, Shorokh, Natalia, Naumchik, Irina V, Volleth, Marianne, Schreyer, Isolde, Nelle, Heike, Stumm, Markus, Wegner, Rolf-Dieter, Reising-Ackermann, Gisela, Merkas, Martina, Brecevic, Lukretija, Martin, Thomas, Rodríguez, Laura, Bhatt, Samarth, Ziegler, Monika, Kreskowski, Katharina, Weise, Anja, Sazci, Ali, Vorsanova, Svetlana, Cioffi, Marcelo de Bello, Ergul, Emel

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Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations von Dörk, Thilo, Bendix-Waltes, Regina, Wegner, Rolf-Dieter, Stumm, Markus

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Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis von Stumm, Markus, Klopocki, Eva, Gasiorek‐Wiens, Adam, Knoll, Ute, Wirjadi, Deni, Sarioglu, Nanette, Wegner, Rolf‐Dieter, Tönnies, Holger

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Fetal 46,XX/69,XXY mixoploidy: origin and confirmation by analysis of fetal urine cells von Wegner, Rolf-Dieter, Kistner, Gerd, Becker, Rolf, Stumm, Markus, Knoll, Ute, Entezami, Michael, Trimborn, Marc

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Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13 von Trimborn, Marc, Wegner, Rolf-Dieter, Tönnies, Holger, Sarioglu, Nanette, Albig, Matthias, Neitzel, Heidemarie

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Prenatal diagnosis of fetal trisomy 6 mosaicism and phenotype of the affected newborn von Wegner, Rolf‐Dieter, Entezami, Michael, Knoll, Ute, Horn, Denise, Sohl, Susanne, Becker, Rolf

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HOM study and parameter calculation of the TESLA cavity model von 曾日华 SCHUH Marcel GERIGK Frank WEGNER Rolf 潘卫民 王光伟 刘熔

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Classification of Fanconi Anemia Patients by Complementation Analysis: Evidence for a Fifth Genetic Subtype von Joenje, Hans, Foe, Jerome R.Lo Ten, Oostra, Anneke B., Berkel, Carola G.M. van, Rooimans, Martin A., Schroeder-Kurth, Traute, Wegner, Rolf-Dieter, Gille, Johan J.P., Buchwald, Manuel, Arwert, Fre

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Characterization of cell cycle checkpoint responses after ionizing radiation in Nijmegen breakage syndrome cells von YAMAZAKI, V, WEGNER, R.-D, KIRCHGESSNER, C. U

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Small Supernumerary Marker Chromosomes 1 With a Normal Phenotype von Liehr, Thomas, Wegner, Rolf-Dieter, Stumm, Markus, Martin, Thomas, Gillessen-Kaesbach, Gabriele, Kosyakova, Nadezda, Ewers, Elisabeth, Hamid, Ahmed Basheer, von Eggeling, Ferdinand, Hentschel, Julia, Ziegler, Monika, Weise, Anja

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High-Power Test of Two Prototype X-Band Accelerating Structures Based on SwissFEL Fabrication Technology von Millar, William L., Grudiev, Alexej, Wuensch, Walter, Lasheras, Nuria Catalan, McMonagle, Gerard, Zennaro, Riccardo, Craievich, Paolo, Bopp, Markus, Lucas, Thomas G., Volpi, Matteo, Paszkiewicz, Jan, Edwards, Amelia, Wegner, Rolf, Bursali, Hikmet, Woolley, Benjamin, Magazinik, Anastasiya, Syratchev, Igor, Vnuchenko, Anna, Pitman, Samantha, Romano, Veronica del Pozo, Caballero, David Ba non, Burt, Graeme

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Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins von Grömminger, Sebastian, Yagmur, Erbil, Erkan, Sanli, Nagy, Sándor, Schöck, Ulrike, Bonnet, Joachim, Smerdka, Patricia, Ehrich, Mathias, Wegner, Rolf-Dieter, Hofmann, Wera, Stumm, Markus

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The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p von Waisfisz, Quinten, Altay, Cigdem, Leegwater, Peter A., de Winter, Johan P., Komatsu, Kenshi, Evans, Gareth R., Wegner, Rolf-Dieter, Reis, André, Joenje, Hans, Arwert, Fré, Mathew, Christopher G., Pronk, Jan C., Saar, Kathrin, Morgan, Neil V., Digweed, Martin

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