Not logged in DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders Lessel, Ivana; Baresic, Anja; Chinn, Ivan K.; May, Jonathan; Goenka, Anu; Chandler, Kate E.; Posey, Jennifer E.; Afenjar, Alexandra; Averdunk, Luisa; Bedeschi, Maria Francesca; Besnard, Thomas; Brager, Rae; Brick, Lauren; Brugger, Melanie; Brunet, Theresa; Byrne, Susan; de la Calle-Martin, Oscar; Capra, Valeria; Cardenas, Paul; Chappe, Celine; Chong, Hey J.; Cogne, Benjamin; Conboy, Erin; Cope, Heidi; Courtin, Thomas; Deb, Wallid; Dilena, Robertino; Dubourg, Christele; Elgizouli, Magdeldin; Fernandes, Erica; Fitzgerald, Kristi K.; Gangi, Silvana; George-Abraham, Jaya K.; Gucsavas-Calikoglu, Muge; Haack, Tobias B.; Hadonou, Medard; Hanker, Britta; Huning, Irina; Iascone, Maria; Isidor, Bertrand; Jarvela, Irma; Jin, Jay J.; Jorge, Alexander A. L.; Josifova, Dragana; Kalinauskiene, Ruta; Kamsteeg, Erik-Jan; Keren, Boris; Kessler, Elena; Koelbel, Heike; Kozenko, Mariya; Kubisch, Christian; Kuechler, Alma; Leal, Suzanne M.; Leppala, Juha; Luu, Sharon M.; Lyon, Gholson J.; Madan-Khetarpal, Suneeta; Mancardi, Margherita; Marchi, Elaine; Mehta, Lakshmi; Menendez, Beatriz; Morel, Chantal F.; Harasink, Sue Moyer; Nevay, Dayna-Lynn; Nigro, Vincenzo; Odent, Sylvie; Oegema, Renske; Pappas, John; Pastore, Matthew T.; Perilla-Young, Yezmin; Platzer, Konrad; Powell-Hamilton, Nina; Rabin, Rachel; Rekab, Aisha; Rezende, Raissa C.; Robert, Leema; Romano, Ferruccio; Scala, Marcello; Poths, Karin; Schrauwen, Isabelle; Sebastian, Jessica; Short, John; Sidlow, Richard; Sullivan, Jennifer; Szakszon, Katalin; Tan, Queenie K. G.; Wagner, Matias; Wieczorek, Dagmar; Yuan, Bo; Maeding, Nicole; Strunk, Dirk; Begtrup, Amber; Banka, Siddharth; Lupski, James R.; Tolosa, Eva; Lessel, Davor Share Save
Clinical and functional consequences of GRIA variants in patients with neurological diseases XiangWei, Wenshu; Perszyk, Riley E.; Liu, Nana; Xu, Yuchen; Bhattacharya, Subhrajit; Shaulsky, Gil H.; Smith-Hicks, Constance; Fatemi, Ali; Fry, Andrew E.; Chandler, Kate; Wang, Tao; Vogt, Julie; Cohen, Julie S.; Paciorkowski, Alex R.; Poduri, Annapurna; Zhang, Yuehua; Wang, Shuang; Wang, Yuping; Zhai, Qiongxiang; Fang, Fang; Leng, Jie; Garber, Kathryn; Myers, Scott J.; Jauss, Robin-Tobias; Park, Kristen L.; Benke, Timothy A.; Lemke, Johannes R.; Yuan, Hongjie; Jiang, Yuwu; Traynelis, Stephen F. Share Save
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies Accogli, Andrea; Zaki, Maha S.; Al-Owain, Mohammed; Otaif, Mansour Y.; Jackson, Adam; Argilli, Emanuela; Chandler, Kate E.; De Goede, Christian G. E. L.; Cora, Tulun; Alvi, Javeria Raza; Eslahi, Atieh; Mohajeri, Mahsa Sadat Asl; Ashtiani, Setareh; Au, P. Y. Billie; Scocchia, Alicia; Alakurtti, Kirsi; Pagnamenta, Alistair T.; Toosi, Mehran Beiraghi; Karimiani, Ehsan Ghayoor; Mojarrad, Majid; Arab, Fatemeh; Duymus, Fahrettin; Scantlebury, Morris H.; Yesil, Gozde; Rosenfeld, Jill Anne; Turkyilmaz, Ayberk; Sager, Safiye Gunes; Sultan, Tipu; Ashrafzadeh, Farah; Zahra, Tatheer; Rahman, Fatima; Maqbool, Shazia; Abdel-Hamid, Mohamed S.; Issa, Mahmoud Y.; Efthymiou, Stephanie; Bauer, Peter; Zifarelli, Giovanni; Salpietro, Vincenzo; Al-Hassnan, Zuhair; Banka, Siddharth; Sherr, Elliot H.; Gleeson, Joseph G.; Striano, Pasquale; Houlden, Henry; Genomics England Res Consortium, Mariasavina; Severino, Mariasavina; Maroofian, Reza Share Save
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 Jackson, Adam; Lin, Sheng-Jia; Jones, Elizabeth A.; Chandler, Kate E.; Orr, David; Moss, Celia; Haider, Zahra; Ryan, Gavin; Holden, Simon; Harrison, Mike; Burrows, Nigel; Jones, Wendy D.; Loveless, Mary; Petree, Cassidy; Stewart, Helen; Low, Karen; Donnelly, Deirdre; Lovell, Simon; Drosou, Konstantina; Varshney, Gaurav K.; Banka, Siddharth Share Save
Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defects Jackson, Adam; Moss, Celia; Chandler, Kate E.; Balboa, Pablo Lopez; Bageta, Maria L.; Petrof, Gabriela; Martinez, Anna E.; Liu, Lu; Guy, Alyson; Mellerio, Jemima E.; Lee, John Y. W.; Ogboli, Malobi; Ryan, Gavin; McGrath, John A.; Banka, Siddharth Share Save
Clinical and genetic findings in TRPM1-related congenital stationary night blindness Iosifidis, Christos; Liu, Jingshu; Gale, Theodora; Ellingford, Jamie M.; Campbell, Christopher; Ingram, Stuart; Chandler, Kate; Parry, Neil R. A.; Black, Graeme C.; Sergouniotis, Panagiotis, I Share Save
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency Fasham, James; Lin, Siying; Ghosh, Promita; Radio, Francesca Clementina; Farrow, Emily G.; Thiffault, Isabelle; Kussman, Jennifer; Zhou, Dihong; Hemming, Rick; Zahka, Kenneth; Chioza, Barry A.; Rawlins, Lettie E.; Wenger, Olivia K.; Gunning, Adam C.; Pizzi, Simone; Onesimo, Roberta; Zampino, Giuseppe; Barker, Emily; Osawa, Natasha; Rodriguez, Megan Christine; Neuhann, Teresa M.; Zackai, Elaine H.; Keena, Beth; Capasso, Jenina; Levin, Alex, V; Bhoj, Elizabeth; Li, Dong; Hakonarson, Hakon; Wentzensen, Ingrid M.; Jackson, Adam; Chandler, Kate E.; Coban-Akdemir, Zeynep H.; Posey, Jennifer E.; Banka, Siddharth; Lupski, James R.; Sheppard, Sarah E.; Tartaglia, Marco; Triggs-Raine, Barbara; Crosby, Andrew H.; Baple, Emma L. Share Save
Further delineation of the clinical spectrum of White-Sutton syndrome: 12 new individuals and a review of the literature Murch, Oliver; Jain, Vani; Benneche, Andreas; Metcalfe, Kay; Hobson, Emma; Prescott, Katrina; Chandler, Kate; Ghali, Neeti; Carmichael, Jenny; Foulds, Nicola C.; Paulsen, Julie; Smeland, Marie F.; Berland, Siren; Fry, Andrew E. Share Save
Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders Molina-Ramirez, Leslie Patricia; Kyle, Claire; Ellingford, Jamie M.; Wright, Ronnie; Taylor, Algy; Bhaskar, Sanjeev S.; Campbell, Christopher; Jackson, Harriet; Fairclough, Adele; Rousseau, Abigail; Burghel, George J.; Dutton, Laura; Banka, Siddharth; Briggs, Tracy A.; Clayton-Smith, Jill; Douzgou, Sofia; Jones, Elizabeth A.; Kingston, Helen M.; Kerr, Bronwyn; Ealing, John; Somarathi, Suresh; Chandler, Kate E.; Stuart, Helen M.; Burkitt-Wright, Emma M. M.; Newman, William G.; Bruce, Iain A.; Black, Graeme C.; Gokhale, David Share Save
De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females Polla, D. L.; Bhoj, E. J.; Verheij, J. B. G. M.; Wassink-Ruiter, J. S. Klein; Reis, A.; Deshpande, C.; Gregor, A.; Hill-Karfe, K.; Vulto-van Silfhout, A. T.; Pfundt, R.; Bongers, E. M. H. F.; Hakonarson, H.; Berland, S.; Gradek, G.; Banka, S.; Chandler, K.; Gompertz, L.; Huffels, S. C.; Stumpel, C. T. R. M.; Wennekes, R.; Stegmann, A. P. A.; Reardon, W.; Leenders, E. K. S. M.; de Vries, B. B. A.; Li, D.; Zackai, E.; Ragge, N.; Lynch, S. A.; Cuddapah, S.; van Bokhoven, H.; Zweier, C.; de Brouwer, A. P. M. Share Save
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females Radio, Francesca Clementina; Pang, Kaifang; Ciolfi, Andrea; Levy, Michael A.; Hernandez-Garcia, Andres; Pedace, Lucia; Pantaleoni, Francesca; Liu, Zhandong; de Boer, Elke; Jackson, Adam; Bruselles, Alessandro; McConkey, Haley; Stellacci, Emilia; Lo Cicero, Stefania; Motta, Marialetizia; Carrozzo, Rosalba; Dentici, Maria Lisa; McWalter, Kirsty; Desai, Megha; Monaghan, Kristin G.; Telegrafi, Aida; Philippe, Christophe; Vitobello, Antonio; Au, Margaret; Grand, Katheryn; Sanchez-Lara, Pedro A.; Baez, Joanne; Lindstrom, Kristin; Kulch, Peggy; Sebastian, Jessica; Madan-Khetarpal, Suneeta; Roadhouse, Chelsea; MacKenzie, Jennifer J.; Monteleone, Berrin; Saunders, Carol J.; Cuevas, July K. Jean; Cross, Laura; Zhou, Dihong; Hartley, Taila; Sawyer, Sarah L.; Monteiro, Fabiola Paoli; Secches, Tania Vertemati; Kok, Fernando; Schultz-Rogers, Laura E.; Macke, Erica L.; Morava, Eva; Klee, Eric W.; Kemppainen, Jennifer; Iascone, Maria; Selicorni, Angelo; Tenconi, Romano; Amor, David J.; Pais, Lynn; Gallacher, Lyndon; Turnpenny, Peter D.; Stals, Karen; Ellard, Sian; Cabet, Sara; Lesca, Gaetan; Pascal, Joset; Steindl, Katharina; Ravid, Sarit; Weiss, Karin; Castle, Alison M. R.; Carter, Melissa T.; Kalsner, Louisa; de Vries, Bert B. A.; van Bon, Bregje W.; Wevers, Marijke R.; Pfundt, Rolph; Stegmann, Alexander P. A.; Kerr, Bronwyn; Kingston, Helen M.; Chandler, Kate E.; Sheehan, Willow; Elias, Abdallah F.; Shinde, Deepali N.; Towne, Meghan C.; Robin, Nathaniel H.; Goodloe, Dana; Vanderver, Adeline; Sherbini, Omar; Bluske, Krista; Hagelstrom, R. Tanner; Zanus, Caterina; Faletra, Flavio; Musante, Luciana; Kurtz-Nelson, Evangeline C.; Earl, Rachel K.; Anderlid, Britt-Marie; Morin, Gilles; van Slegtenhorst, Marjon; Diderich, Karin E. M.; Brooks, Alice S.; Gribnau, Joost; Boers, Ruben G.; Finestra, Teresa Robert; Carter, Lauren B.; Rauch, Anita; Gasparini, Paolo; Boycott, Kym M.; Barakat, Tahsin Stefan; Graham, John M., Jr.; Faivre, Laurence; Banka, Siddharth; Wang, Tianyun; Eichler, Evan E.; Priolo, Manuela; Dallapiccola, Bruno; Vissers, Lisenka E. L. M.; Sadikovic, Bekim; Scott, Daryl A.; Holder, Jimmy Lloyd, Jr.; Tartaglia, Marco Share Save
ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy Hyder, Zerin; Van Paesschen, Wim; Sabir, Ataf; Sansbury, Francis H.; Burke, Katherine B.; Khan, Naz; Chandler, Kate E.; Cooper, Nicola S.; Wright, Ronnie; McHale, Edward; Van Esch, Hilde; Banka, Siddharth Share Save
KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants (vol 21, 10.1038/s41436-018-0259-2, 2019) Kennedy, Joanna; Goudie, David; Blair, Edward; Chandler, Kate; Joss, Shelagh; McKay, Victoria; Green, Andrew; Armstrong, Ruth; Lees, Melissa; Kamien, Benjamin; Hopper, Bruce; Tan, Tiong Yang; Yap, Patrick; Stark, Zornitza; Okamoto, Nobuhiko; Miyake, Noriko; Matsumoto, Naomichi; Macnamara, Ellen; Murphy, Jennifer L.; McCormick, Elizabeth; Hakonarson, Hakon; Falk, Marni J.; Li, Dong; Blackburn, Patrick; Klee, Eric; Babovic-Vuksanovic, Dusica; Schelley, Susan; Hudgins, Louanne; Kant, Sarina; Isidor, Bertrand; Cogne, Benjamin; Bradbury, Kimberley; Williams, Mark; Patel, Chirag; Heussler, Helen; Duff-Farrier, Celia; Lakeman, Phillis; Scurr, Ingrid; Kini, Usha; Elting, Mariet; Reijnders, Margot; Schuurs-Hoeijmakers, Janneke; Wafik, Mohamed; Blomhoff, Anne; Ruivenkamp, Claudia A. L.; Nibbeling, Esther; Dingemans, Alexander J. M.; Douine, Emilie D.; Nelson, Stanley F.; Hempel, Maja; Bierhals, Tatjana; Lessel, Davor; Johannsen, Jessika; Arboleda, Valerie A.; Newbury-Ecob, Ruth Share Save
Contribution of retrotransposition to developmental disorders Gardner, Eugene J.; Prigmore, Elena; Gallone, Giuseppe; Danecek, Petr; Samocha, Kaitlin E.; Handsaker, Juliet; Gerety, Sebastian S.; Ironfield, Holly; Short, Patrick J.; Sifrim, Alejandro; Singh, Tarjinder; Chandler, Kate E.; Clement, Emma; Lachlan, Katherine L.; Prescott, Katrina; Rosser, Elisabeth; FitzPatrick, David R.; Firth, Helen, V; Hurles, Matthew E. Share Save
Prenatal Exome Sequencing Analysis in Fetal Structural Anomalies Detected by Ultrasonography (PAGE): A Cohort Study Lord, Jenny; McMullan, Dominic J.; Eberhardt, Ruth Y.; Rinck, Gabriele; Hamilton, Susan J.; Quinlan-Jones, Elizabeth; Prigmore, Elena; Keelagher, Rebecca; Best, Sunayna K.; Carey, Georgina K.; Mellis, Rhiannon; Robart, Sarah; Berry, Ian R.; Chandler, Kate E.; Cilliers, Deirdre; Cresswell, Lara; Edwards, Sandra L.; Gardiner, Carol; Henderson, Alex; Holden, Simon T.; Homfray, Tessa; Lester, Tracy; Lewis, Rebecca A.; Newbury-Ecob, Ruth; Prescott, Katrina; Quarrell, Oliver W.; Ramsden, Simon C.; Roberts, Eileen; Tapon, Dagmar; Tooley, Madeleine J.; Vasudevan, Pradeep C.; Weber, Astrid P.; Wellesley, Diana G.; Westwood, Paul; White, Helen; Parker, Michael; Williams, Denise; Jenkins, Lucy; Scott, Richard H.; Kilby, Mark D.; Chitty, Lyn S.; Hurles, Matthew E.; Maher, Eamonn R. Share Save
KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants Kennedy, Joanna; Goudie, David; Blair, Edward; Chandler, Kate; Joss, Shelagh; McKay, Victoria; Green, Andrew; Armstrong, Ruth; Lees, Melissa; Kamien, Benjamin; Hopper, Bruce; Tan, Tiong Yang; Yap, Patrick; Stark, Zornitza; Okamoto, Nobuhiko; Miyake, Noriko; Matsumoto, Naomichi; Macnamara, Ellen; Murphy, Jennifer L.; McCormick, Elizabeth; Hakonarson, Hakon; Falk, Marni J.; Li, Dong; Blackburn, Patrick; Klee, Eric; Babovic-Vuksanovic, Dusica; Schelley, Susan; Hudgins, Louanne; Kant, Sarina; Isidor, Bertrand; Cogne, Benjamin; Bradbury, Kimberley; Williams, Mark; Patel, Chirag; Heussler, Helen; Duff-Farrier, Celia; Lakeman, Phillis; Scurr, Ingrid; Kini, Usha; Elting, Mariet; Reijnders, Margot; Schuurs-Hoeijmakers, Janneke; Wafik, Mohamed; Blomhoff, Anne; Ruivenkamp, Claudia A. L.; Nibbeling, Esther; Dingemans, Alexander J. M.; Douine, Emilie D.; Nelson, Stanley F.; Arboleda, Valerie A.; Newbury-Ecob, Ruth Share Save
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study Lord, Jenny; McMullan, Dominic J.; Eberhardt, Ruth Y.; Rinck, Gabriele; Hamilton, Susan J.; Quinlan-Jones, Elizabeth; Prigmore, Elena; Keelagher, Rebecca; Best, Sunayna K.; Carey, Georgina K.; Mellis, Rhiannon; Robart, Sarah; Berry, Ian R.; Chandler, Kate E.; Cilliers, Deirdre; Cresswell, Lara; Edwards, Sandra L.; Gardiner, Carol; Henderson, Alex; Holden, Simon T.; Homfray, Tessa; Lester, Tracy; Lewis, Rebecca A.; Newbury-Ecob, Ruth; Prescott, Katrina; Quarrell, Oliver W.; Ramsden, Simon C.; Roberts, Eileen; Tapon, Dagmar; Tooley, Madeleine J.; Vasudevan, Pradeep C.; Weber, Astrid P.; Wellesley, Diana G.; Westwood, Paul; White, Helen; Parker, Michael; Williams, Denise; Jenkins, Lucy; Scott, Richard H.; Kilby, Mark D.; Chitty, Lyn S.; Hurles, Matthew E.; Maher, Eamonn R.; Bateman, Mark; Campbell, Carolyn; Campbell, Jenni; Carey, Georgina; Cohen, Kelly; Collingwood, Emma; Constantinou, Panayiotis; Delmege, Catherine; Ellis, Richard; Evans, Jerry; Everett, Thomas; Pinto, Clare Ferreira; Forrester, Natalie; Fowler, Emma; Gardiner, Carol; Hamilton, Susan; Healey, Karen; Hudson, Rebecca; Marton, Tamas; Mehta, Sarju; Park, Soo-Mi; Prigmore, Elena; Quarrell, Oliver; Ramsden, Simon; Rowland, Jayne; Steer, James; Taylor, Emma Jane; Wilson, Elizabeth Share Save
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder Reijnders, Margot R. F.; Miller, Kerry A.; Alvi, Mohsan; Goos, Jacqueline A. C.; Lees, Melissa M.; de Burca, Anna; Henderson, Alex; Kraus, Alison; Mikat, Barbara; de Vries, Bert B. A.; Isidor, Bertrand; Kerr, Bronwyn; Marcelis, Carlo; Schluth-Bolard, Caroline; Deshpande, Charu; Ruivenkamp, Claudia A. L.; Wieczorek, Dagmar; Baralle, Diana; Blair, Edward M.; Engels, Hartmut; Luedecke, Hermann-Josef; Eason, Jacqueline; Santen, Gijs W. E.; Clayton-Smith, Jill; Chandler, Kate; Tatton-Brown, Katrina; Payne, Katelyn; Helbig, Katherine; Radtke, Kelly; Nugent, Kimberly M.; Cremer, Kirsten; Strom, Tim M.; Bird, Lynne M.; Sinnema, Margje; Bitner-Glindzicz, Maria; van Dooren, Marieke F.; Alders, Marielle; Koopmans, Marije; Brick, Lauren; Kozenko, Mariya; Harline, Megan L.; Klaassens, Merel; Steinraths, Michelle; Cooper, Nicola S.; Edery, Patrick; Yap, Patrick; Terhal, Paulien A.; van der Spek, Peter J.; Lakeman, Phillis; Taylor, Rachel L.; Littlejohn, Rebecca O.; Pfundt, Rolph; Mercimek-Andrews, Saadet; Stegmann, Alexander P. A.; Kant, Sarina G.; McLean, Scott; Joss, Shelagh; Swagemakers, Sigrid M. A.; Douzgou, Sofia; Wall, Steven A.; Kury, Sebastien; Calpena, Eduardo; Koelling, Nils; McGowan, Simon J.; Twigg, Stephen R. F.; Mathijssen, Irene M. J.; Nellaker, Christoffer; Brunner, Han G.; Wilkie, Andrew O. M. Share Save
ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder Cuvertino, Sara; Stuart, Helen M.; Chandler, Kate E.; Roberts, Neil A.; Armstrong, Ruth; Bernardini, Laura; Bhaskar, Sanjeev; Callewaert, Bert; Clayton-Smith, Jill; Hernando Davalillo, Cristina; Deshpande, Charu; Devriendt, Koenraad; Digilio, Maria C.; Dixit, Abhijit; Edwards, Matthew; Friedman, Jan M.; Gonzalez-Meneses, Antonio; Joss, Shelagh; Kerr, Bronwyn; Lampe, Anne Katrin; Langlois, Sylvie; Lennon, Rachel; Loget, Philippe; Ma, David Y. T.; McGowan, Ruth; Des Medt, Maryse; O'Sullivan, James; Odent, Sylvie; Parker, Michael J.; Pebrel-Richard, Celine; Petit, Florence; Stark, Zornitza; Stockler-Ipsiroglu, Sylvia; Tinschert, Sigrid; Vasudevan, Pradeep; Villa, Olaya; White, Susan M.; Zahir, Farah R.; Woolf, Adrian S.; Banka, Siddharth Share Save
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature Reijnders, Margot R. F.; Janowski, Robert; Alvi, Mohsan; Self, Jay E.; van Essen, Ton J.; Vreeburg, Maaike; Rouhl, Rob P. W.; Stevens, Servi J. C.; Stegmann, Alexander P. A.; Schieving, Jolanda; Pfundt, Rolph; van Dijk, Katinke; Smeets, Eric; Stumpel, Connie T. R. M.; Bok, Levinus A.; Cobben, Jan Maarten; Engelen, Marc; Mansour, Sahar; Whiteford, Margo; Chandler, Kate E.; Douzgou, Sofia; Cooper, Nicola S.; Tan, Ene-Choo; Foo, Roger; Lai, Angeline H. M.; Rankin, Julia; Green, Andrew; Loennqvist, Tuula; Isohanni, Pirjo; Williams, Shelley; Ruhoy, Ilene; Carvalho, Karen S.; Dowling, James J.; Lev, Dorit L.; Sterbova, Katalin; Lassuthova, Petra; Neupauerova, Jana; Waugh, Jeff L.; Keros, Sotirios; Clayton-Smith, Jill; Smithson, Sarah F.; Brunner, Han G.; van Hoeckel, Ceciel; Anderson, Mel; Clowes, Virginia E.; Siu, Victoria Mok; Selber, Paulo; Leventer, Richard J.; Nellaker, Christoffer; Niessing, Dierk; Hunt, David; Baralle, Diana Share Save
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