A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria von van der Sluijs, Pleuntje J., Alders, Marielle, Dingemans, Alexander J. M., Parbhoo, Kareesma, van Bon, Bregje W., Dempsey, Jennifer C., Doherty, Dan, den Dunnen, Johan T., Gerkes, Erica H., Milller, Ilana M., Moortgat, Stephanie, Regier, Debra S., Ruivenkamp, Claudia A. L., Schmalz, Betsy, Smol, Thomas, Stuurman, Kyra E., Vincent-Delorme, Catherine, de Vries, Bert B. A., Sadikovic, Bekim, Hickey, Scott E., Rosenfeld, Jill A., Maystadt, Isabelle, Santen, Gijs W. E.

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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition von Picketts, D, Mirzaa, G, Yan, K, Relator, R, Timpano, S, Yalcin, B, Collins, S, Ziegler, A, Pao, E, Oyama, N, Brischoux-Boucher, E, Piard, J, Monaghan, K, Sacoto, MG, Dobyns, W, Park, K, Fernández-Mayoralas, D, Fernández-Jaén, A, Jayakar, P, Brusco, A, Antona, V, Giorgio, E, Kvarnung, M, Isidor, B, Conrad, S, Cogné, B, Deb, W, Stuurman, KE, Sterbova, K, Smal, N, Weckhuysen, S, Oegema, R, Innes, M, Latsko, M, Ben-Omran, T, Yeh, R, Kruer, M, Bakhtiari, S, Papavasiliou, A, Moutton, S, Nambot, S, Chanprasert, S, Paolucci, S, Miller, K, Burton, B, Kim, K, O'Heir, E, Bruwer, Z, Donald, K, Kleefstra, T, Goldstein, A, Angle, B, Bontempo, K, Miny, P, Joset, P, Demurger, F, Hobson, E, Pang, L, Carpenter, L, Li, D, Bonneau, D, Sadikovic, B

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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition von Picketts, David, Mirzaa, Ghayda, Yan, Keqin, Relator, Raissa, Timpano, Sara, Yalcin, Binnaz, Collins, Stephan, Ziegler, Alban, Pao, Emily, Oyama, Nora, Brischoux-Boucher, Elise, Piard, Juliette, Monaghan, Kristin, Sacoto, Maria Guillen, Dobyns, William, Park, Kristen, Fernández-Mayoralas, Daniel, Fernández-Jaén, Alberto, Jayakar, Parul, Brusco, Alfredo, Antona, Vincenzo, Giorgio, Elisa, Kvarnung, Malin, Isidor, Bertrand, Conrad, Solène, Cogné, Benjamin, Deb, Wallid, Stuurman, K E, Sterbova, Katalin, Smal, Noor, Weckhuysen, Sarah, Oegema, Renske, Innes, Micheil, Latsko, Maeson, Ben-Omran, Tawfeg, Yeh, Rebecca, Kruer, Michael, Bakhtiari, Somayeh, Papavasiliou, Antigone, Moutton, Sébastien, Nambot, Sophie, Chanprasert, Sirisak, Paolucci, Sarah, Miller, Kait, Burton, Barbara, Kim, Katherine, O'Heir, Emily, Bruwer, Zandre, Donald, Kirsten, Kleefstra, Tjitske, Goldstein, Amy, Angle, Brad, Bontempo, Kelly, Miny, Peter, Joset, Pascal, Demurger, Florence, Hobson, Emma, Pang, Lewis, Carpenter, Lori, Li, Dong, Bonneau, Dominique, Sadikovic, Bekim

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Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, van de Kamp, Jiddeke, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Lüttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Schrier Vergano, Samantha A, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla Sirera, Natàlia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon, Bhoj, Elizabeth J, Universitat Autònoma de Barcelona

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Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, van de Kamp, Jiddeke, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Lüttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Schrier Vergano, Samantha A, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla Sirera, Natàlia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon, Bhoj, Elizabeth J, Universitat Autònoma de Barcelona

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Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, Kamp, Jiddeke van de, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Luttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Thomas, Jennifer Muncy, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vollo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Vergano, Samantha A. Schrier, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Allen, Margot van, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla, Natalia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon H, Bhoj, Elizabeth J

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Efficacy and safety of an attenuated live QX-like infectious bronchitis virus strain as a vaccine for chickens von Geerligs, H.J, Boelm, G.J, Meinders, C.A.M, Stuurman, B.G.E, Symons, J, Tarres-Call, J, Bru, T, Vila, R, Mombarg, M, Karaca, K, Wijmenga, W, Kumar, M

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Translatability of preclinical to early clinical tolerable and pharmacologically active dose ranges for central nervous system active drugs von Ferreira, Guilherme S., Dijkstra, Francis M., Veening-Griffioen, Désirée H., Boon, Wouter P. C., Schellekens, Huub, Moors, Ellen H. M., van Meer, Peter J. K., Stuurman, Frederik E., van Gerven, Joop M. A.

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The detection of a strong episignature for Chung–Jansen syndrome, partially overlapping with Börjeson–Forssman–Lehmann and White–Kernohan syndromes von Vos, Niels, Haghshenas, Sadegheh, van der Laan, Liselot, Russel, Perle K. M., Rooney, Kathleen, Levy, Michael A., Relator, Raissa, Kerkhof, Jennifer, McConkey, Haley, Maas, Saskia M., Vissers, Lisenka E. L. M., de Vries, Bert B. A., Pfundt, Rolph, Elting, Mariet W., van Hagen, Johanna M., Verbeek, Nienke E., Jongmans, Marjolijn C. J., Lakeman, Phillis, Rumping, Lynne, Bosch, Danielle G. M., Vitobello, Antonio, Thauvin-Robinet, Christel, Faivre, Laurence, Nambot, Sophie, Garde, Aurore, Willems, Marjolaine, Genevieve, David, Nicolas, Gaël, Busa, Tiffany, Toutain, Annick, Gérard, Marion, Bizaoui, Varoona, Isidor, Bertrand, Merla, Giuseppe, Accadia, Maria, Schwartz, Charles E., Ounap, Katrin, Hoffer, Mariëtte J. V., Nezarati, Marjan M., van den Boogaard, Marie-José H., Tedder, Matthew L., Rogers, Curtis, Brusco, Alfredo, Ferrero, Giovanni B., Spodenkiewicz, Marta, Sidlow, Richard, Mussa, Alessandro, Trajkova, Slavica, McCann, Emma, Mroczkowski, Henry J., Jansen, Sandra, Donker-Kaat, Laura, Duijkers, Floor A. M., Stuurman, Kyra E., Mannens, Marcel M. A. M., Alders, Mariëlle, Henneman, Peter, White, Susan M., Sadikovic, Bekim, van Haelst, Mieke M.

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Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype von Tatton-Brown, Katrina, Murray, Anne, Hanks, Sandra, Douglas, Jenny, Armstrong, Ruth, Banka, Siddharth, Bird, Lynne M., Clericuzio, Carol L., Cormier-Daire, Valerie, Cushing, Tom, Flinter, Frances, Jacquemont, Marie-Line, Joss, Shelagh, Kinning, Esther, Lynch, Sally Ann, Magee, Alex, McConnell, Vivienne, Medeira, Ana, Ozono, Keiichi, Patton, Michael, Rankin, Julia, Shears, Debbie, Simon, Marleen, Splitt, Miranda, Strenger, Volker, Stuurman, Kyra, Taylor, Clare, Titheradge, Hannah, Van Maldergem, Lionel, Temple, I. Karen, Cole, Trevor, Seal, Sheila, Rahman, Nazneen

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The effects of an online decision aid to support the reproductive decision‐making process of genetically at risk couples—A pilot study von Severijns, Yil, Heijmans, Maartje W. F., Die‐Smulders, Christine E. M., Bijlsma, Emilia K., Corsten‐Janssen, Nicole, Joosten, Sara J. R., Kuijk, Sander M. J., Lichtenbelt, Klaske D., Ottenheim, Cecile P. E., Stuurman, Kyra E., Tan‐Sindhunata, Gita M. B., Vries, Hein, Osch, Liesbeth A. D. M.

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The detection of a strong episignature for Chung-Jansen syndrome, partially overlapping with Börjeson-Forssman-Lehmann and White-Kernohan syndromes von Vos, Niels, Haghshenas, Sadegheh, van der Laan, Liselot, Russel, Perle K M, Rooney, Kathleen, Levy, Michael A, Relator, Raissa, Kerkhof, Jennifer, McConkey, Haley, Maas, Saskia M, Vissers, Lisenka E L M, de Vries, Bert B A, Pfundt, Rolph, Elting, Mariet W, van Hagen, Johanna M, Verbeek, Nienke E, Jongmans, Marjolijn C J, Lakeman, Phillis, Rumping, Lynne, Bosch, Danielle G M, Vitobello, Antonio, Thauvin-Robinet, Christel, Faivre, Laurence, Nambot, Sophie, Garde, Aurore, Willems, Marjolaine, Genevieve, David, Nicolas, Gaël, Busa, Tiffany, Toutain, Annick, Gérard, Marion, Bizaoui, Varoona, Isidor, Bertrand, Merla, Giuseppe, Accadia, Maria, Schwartz, Charles E, Ounap, Katrin, Hoffer, Mariëtte J V, Nezarati, Marjan M, van den Boogaard, Marie-José H, Tedder, Matthew L, Rogers, Curtis, Brusco, Alfredo, Ferrero, Giovanni B, Spodenkiewicz, Marta, Sidlow, Richard, Mussa, Alessandro, Trajkova, Slavica, McCann, Emma, Mroczkowski, Henry J, Jansen, Sandra, Donker-Kaat, Laura, Duijkers, Floor A M, Stuurman, Kyra E, Mannens, Marcel M A M, Alders, Mariëlle, Henneman, Peter, White, Susan M, Sadikovic, Bekim, van Haelst, Mieke M

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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism von Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta M., Kaur, Anupriya, Kaur, Parneet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia M.S., Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra E., Wilke, Martina, Thompson, Michelle L., Bebin, E. Martina, Bijlsma, Emilia K., Hoffer, Mariette J.V., Peeters-Scholte, Cacha, Slavotinek, Anne, Weiss, William A., Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Willaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Yachelevich, Naomi, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Klöckner, Chiara, Kamphausen, Susanne B., Abou Jamra, Rami, Arelin, Maria, Innes, A. Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damian, de Burca, Anna, Kini, Usha, Delatycki, Martin B., Gallacher, Lyndon, Yeung, Alison, Pais, Lynn, Field, Michael, Martin, Ellenore, Charles, Perrine, Courtin, Thomas, Keren, Boris, Iascone, Maria, Cereda, Anna, Poke, Gemma, Abadie, Véronique, Chalouhi, Christel, Parthasarathy, Padmini, Halliday, Benjamin J., Robertson, Stephen P., Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher T.

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Translatability of preclinical to early clinical tolerable and pharmacologically active dose ranges for central nervous system active drugs von Ferreira, Guilherme S, Dijkstra, Francis M, Veening-Griffioen, Désirée H, Boon, Wouter P C, Schellekens, Huub, Moors, Ellen H M, van Meer, Peter J K, Stuurman, Frederik E, van Gerven, Joop M A

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The effects of an online decision aid to support the reproductive decision-making process of genetically at risk couples-A pilot study von Severijns, Yil, Heijmans, Maartje W F, de Die-Smulders, Christine E M, Bijlsma, Emilia K, Corsten-Janssen, Nicole, Joosten, Sara J R, van Kuijk, Sander M J, Lichtenbelt, Klaske D, Ottenheim, Cecile P E, Stuurman, Kyra E, Tan-Sindhunata, Gita M B, de Vries, Hein, van Osch, Liesbeth A D M

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NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns von Stamberger, H, Hammer, TB, Gardella, E, Vlaskamp, DRM, Bertelsen, B, Mandelstam, S, de Lange, I, Zhang, J, Myers, CT, Fenger, C, Afawi, Z, Almanza Fuerte, EP, Andrade, DM, Balcik, Y, Ben Zeev, B, Bennett, MF, Berkovic, SF, Isidor, B, Bouman, A, Brilstra, E, Busk, ØL, Cairns, A, Caumes, R, Chatron, N, Dale, RC, de Geus, C, Edery, P, Gill, D, Granild-Jensen, JB, Gunderson, L, Gunning, B, Heimer, G, Helle, JR, Hildebrand, MS, Hollingsworth, G, Kharytonov, V, Klee, EW, Koeleman, BPC, Koolen, DA, Korff, C, Küry, S, Lesca, G, Lev, D, Leventer, RJ, Mackay, MT, Macke, EL, McEntagart, M, Mohammad, SS, Monin, P, Montomoli, M, Morava, E, Moutton, S, Muir, AM, Parrini, E, Procopis, P, Ranza, E, Reed, L, Reif, PS, Rosenow, F, Rossi, M, Sadleir, LG, Sadoway, T, Schelhaas, HJ, Schneider, AL, Shah, K, Shalev, R, Sisodiya, SM, Smol, T, Stumpel, CTRM, Stuurman, K, Symonds, JD, Mau-Them, FT, Verbeek, N, Verhoeven, JS, Wallace, G, Yosovich, K, Zarate, YA, Zerem, A, Zuberi, SM, Guerrini, R, Mefford, HC, Patel, C, Zhang, Y-H, Møller, RS, Scheffer, IE

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Solar-system-wide significance of Mars polar science von Smith, I, Smith, DE, Hansen, C, McEwen, A, Banfield, D, Becerra, P, Byrne, S, Hvidberg, CS, Hayne, PO, III, JWH, Mellon, M, Horgan, B, Mustard, J, Holt, JW, McCleese, D, Stoker, C, James, P, Putzig, NE, Buhler, P, Crismani, M, Aye, KM, Portyankina, A, Orosei, R, Bramson, A, Sori, M, Sizemore, H, Morgan, G, Schorghofer, N, Berman, D, Obbard, RW, Elmaary, MR, Balme, M, Schmitt, B, Ewing, RC, Guzewich, SD, Levy, J, Łosiak, A, Eke, V, Goldsby, D, Cross, A, Hager, T, Kereszturi, A, Wood, S, Hauber, E, Amos, C, Russell, P, Jaumann, R, Michael, G, Khayat, A, Luizzi, G, Montabone, L, Pankine, A, Phillips-Lander, C, Zacny, K, McAdam, A, Rutledge, A, Bertrand, T, Stillman, D, Yoldi, Z, Young, R, Sam, L, Chojnacki, M, Thomas, P, Karimova, R, Chesal, J, Pascuzzo, A, Osinski, G, Andres, C, Neisch, C, Hibbard, S, Sinha, P, Knightly, JP, Kounaves, S, MacGregor, J, Rabassa, J, McKeown, L, Oliveira, N, Fawdon, P, Gayathri, U, Herny, C, Butcher, F, Perry, M, Hu, R, Mukherjee, S, Banks, ME, Meng, T, Tober, B, Johnson, JC, Dinwiddie, C, Henderson, BL, Rivera-Valentín, E, Nerozzi, S, Petersen, E, Foss, F, Eigenbrode, J, Day, M, Karatekin, Ö, Newman, C, Mischna, M, Streeter, P

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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism von Chopra, M., McEntagart, M., Clayton-Smith, J., Platzer, K., Shukla, A., Girisha, K.M., Kaur, A., Kaur, P., Pfundt, R., Veenstra-Knol, H., Mancini, G.M.S., Cappuccio, G., Brunetti-Pierri, N., Kortum, F., Hempel, M., Denecke, J., Lehman, A., Kleefstra, T., Stuurman, K.E., Wilke, M., Thompson, M.L., Bebin, E.M., Bijlsma, E.K., Hoffer, M.J.V., Peeters-Scholte, C., Slavotinek, A., Weiss, W.A., Yip, T., Hodoglugil, U., Whittle, A., Monda, J., Neira, J., Yang, S., Kirby, A., Pinz, H., Lechner, R., Sleutels, F., Helbig, I., McKeown, S., Helbig, K., Willaert, R., Juusola, J., Semotok, J., Hadonou, M., Short, J., Yachelevich, N., Lala, S., Fernandez-Jaen, A., Pelayo, J.P., Klockner, C., Kamphausen, S.B., Abou Jamra, R., Arelin, M., Innes, A.M., Niskakoski, A., Amin, S., Williams, M., Evans, J., Smithson, S., Smedley, D., Burca, A., Kini, U., Delatycki, M.B., Gallacher, L., Yeung, A., Pais, L., Field, M., Martin, E., Charles, P., Courtin, T., Keren, B., Iascone, M., Cereda, A., Poke, G., Abadie, V., Chalouhi, C., Parthasarathy, P., Halliday, B.J., Robertson, S.P., Lyonnet, S., Amiel, J., Gordon, C.T.

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Recent experimental results with LASS-based ultra-wideband radar systems von Cardwell, K., Giorgi, D., McIntyre, I., Solone, P., Stuurman, K., Zucker, O.S.F., Schultz, E., McGrew, J.

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Recent Experimental Results with LASS-Based Ultra-Wideband Radar Systems von Cardwell, K, Giorgi, D, McIntyre, I, Solone, P, Stuurman, K, Zucker, O S, Schultz, E, McGrew, J, Roessler, N, Bonebright, M

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