檢索結果 - Denayer, Ellen
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Observations on Intelligence and Behavior in 15 Patients with Legius Syndrome 由 Denayer, Ellen, Descheemaeker, Mie-Jef, Stewart, Douglas R, Keymolen, Kathelijn, Plasschaert, Ellen, Ruppert, Sarah L, Snow, Joseph, Thurm, Audrey E, Joseph, Lisa A, Fryns, Jean-Pierre, Legius, Eric
出版 2011Text -
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Spred1 Is Required for Synaptic Plasticity and Hippocampus-Dependent Learning 由 Denayer, Ellen, Ahmed, Tariq, Brems, Hilde, Van Woerden, Geeske, Borgesius, Nils Zuiderveen, Callaerts-Vegh, Zsuzsanna, Yoshimura, Akihiko, Hartmann, Dieter, Elgersma, Ype, D'Hooge, Rudi, Legius, Eric, Balschun, Detlef
出版 2008Text -
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Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M 由 Destouni, Aspasia, Dimitriadou, Eftychia, Masset, Heleen, Debrock, Sophie, Melotte, Cindy, Van Den Bogaert, Kris, Zamani Esteki, Masoud, Ding, Jia, Voet, Thiery, Denayer, Ellen, de Ravel, Thomy, Legius, Eric, Meuleman, Christel, Peeraer, Karen, Vermeesch, Joris R
出版 2018Text -
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Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation 由 Tšuiko, Olga, Vanneste, Michiel, Melotte, Cindy, Ding, Jia, Debrock, Sophie, Masset, Heleen, Peters, Maire, Salumets, Andres, De Leener, Anne, Pirard, Céline, Kluyskens, Candice, Hostens, Katleen, van de Vijver, Arne, Peeraer, Karen, Denayer, Ellen, Vermeesch, Joris Robert, Dimitriadou, Eftychia
出版 2021Text -
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Multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus: a new syndrome 由 Babovic-Vuksanovic, D, Messiaen, Ludwine, Nagel, Christoph, Brems, Hilde, Scheithauer, Bernd, Denayer, Ellen, Mao, Rong, Sciot, Raf, Janowski, Karen M, Schuhmann, Martin U, Claes, Kathleen, Beert, Eline, Garrity, James A, Spinner, Robert J, Stemmer-Rachamimov, Anat, Gavrilova, Ralitza, Van Calenbergh, Frank, Mautner, Victor, Legius, Eric
出版 2012Text -
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Cancer Surveillance in Healthy Carriers of Germline Pathogenic Variants in BRCA1/2: A Review of Secondary Prevention Guidelines 由 Dullens, Boudewijn, de Putter, Robin, Lambertini, Matteo, Toss, Angela, Han, Sileny, Van Nieuwenhuysen, Els, Van Gorp, Toon, Vanderstichele, Adriaan, Van Ongeval, Chantal, Keupers, Machteld, Prevos, Renate, Celis, Valerie, Dekervel, Jeroen, Everaerts, Wouter, Wildiers, Hans, Nevelsteen, Ines, Neven, Patrick, Timmerman, Dirk, Smeets, Ann, Denayer, Ellen, Van Buggenhout, Griet, Legius, Eric, Punie, Kevin
出版 2020Text -
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Legius Syndrome in Fourteen Families 由 Denayer, Ellen, Chmara, Magdalena, Brems, Hilde, Kievit, Anneke Maat, van Bever, Yolande, Van den Ouweland, Ans MW, Van Minkelen, Rick, de Goede-Bolder, Arja, Oostenbrink, Rianne, Lakeman, Phillis, Beert, Eline, Ishizaki, Takuma, Mori, Tomoaki, Keymolen, Kathelijn, Van den Ende, Jenneke, Mangold, Elisabeth, Peltonen, Sirkku, Brice, Glen, Rankin, Julia, Van Spaendonck-Zwarts, Karin Y, Yoshimura, Akihiko, Legius, Eric
出版 2011Text -
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Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation 由 Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.
出版 2018Text -
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Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation 由 Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.
出版 2018Text