Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3 von Brouillard, Pascal, Dupont, Laura, Helaers, Raphael, Coulie, Richard, Tiller, George E, Peeden, Joseph, Colige, Alain, Vikkula, Miikka

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A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation von Hussain, Iram, Patni, Nivedita, Ueda, Masako, Sorkina, Ekaterina, Valerio, Cynthia M, Cochran, Elaine, Brown, Rebecca J, Peeden, Joseph, Tikhonovich, Yulia, Tiulpakov, Anatoly, Stender, Sarah R S, Klouda, Elisabeth, Tayeh, Marwan K, Innis, Jeffrey W, Meyer, Anders, Lal, Priti, Godoy-Matos, Amelio F, Teles, Milena G, Adams-Huet, Beverley, Rader, Daniel J, Hegele, Robert A, Oral, Elif A, Garg, Abhimanyu

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The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings von Gozes, Illana, Patterson, Marc C, Van Dijck, Anke, Kooy, R Frank, Peeden, Joseph N, Eichenberger, Jacob A, Zawacki-Downing, Angela, Bedrosian-Sermone, Sandra

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Valediction von Peeden, Joseph

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Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C‐terminal region of RUNX2 von El‐Gharbawy, Areeg H., Peeden, Joseph N., Lachman, Ralph S., Graham, John M., Moore, Stephen R., Rimoin, David L.

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Familial Clustering of Autoimmune Disorders and Evaluation of Medical Risk Factors in Autism von Comi, Anne M., Zimmerman, Andrew W., Frye, Virginia H., Law, Paul A., Peeden, Joseph N.

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Streptococcal Mediastinitis Following Placement of a Bravo ™ Capsule von Peeden, Joseph, Conner, Anna, Pappano, Dante

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Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP von Van Dijck, Anke, Vulto-van Silfhout, Anneke T., Cappuyns, Elisa, van der Werf, Ilse M., Mancini, Grazia M., Tzschach, Andreas, Bernier, Raphael, Gozes, Illana, Eichler, Evan E., Romano, Corrado, Lindstrand, Anna, Nordgren, Ann, Bakshi, Madhura, Wilson, Meredith, Berman, Yemina, Dickson, Rebecca, Fransen, Erik, Helsmoortel, Céline, Van den Ende, Jenneke, Van der Aa, Nathalie, van de Wijdeven, Marina J., Rosenblum, Jessica, Monteiro, Fabíola, Kok, Fernando, Quercia, Nada, Bowdin, Sarah, Dyment, David, Chitayat, David, Alkhunaizi, Ebba, Boonen, Susanne E., Keren, Boris, Jacquette, Aurelia, Faivre, Laurence, Bezieau, Stephane, Isidor, Bertrand, Rieß, Angelika, Moog, Ute, Lynch, Sally Ann, McVeigh, Terri, Elpeleg, Orly, Smeland, Marie Falkenberg, Fannemel, Madeleine, van Haeringen, Arie, Maas, Saskia M., Veenstra-Knol, H.E., Schouten, Meyke, Willemsen, Marjolein H., Marcelis, Carlo L., Ockeloen, Charlotte, van der Burgt, Ineke, Feenstra, Ilse, van der Smagt, Jasper, Jezela-Stanek, Aleksandra, Krajewska-Walasek, Malgorzata, González-Lamuño, Domingo, Anderlid, Britt-Marie, Malmgren, Helena, Nordenskjöld, Magnus, Hurst, Jane, Metcalfe, Kay, Mansour, Sahar, Lachlan, Katherine, Clayton-Smith, Jill, Hendon, Laura G., Abdulrahman, Omar A., Morrow, Eric, McMillan, Clare, Gerdts, Jennifer, Peeden, Joseph, Schrier Vergano, Samantha A., Valentino, Caitlin, Chung, Wendy K., Ozmore, Jillian R., Bedrosian-Sermone, Sandra, Treat, Kayla, Hughes, Susan Starling, Safina, Nicole, Le Pichon, Jean-Baptiste, McGuire, Marianne, Infante, Elena, Madan-Khetarpal, Suneeta, Desai, Sonal, Benke, Paul, Krokosky, Alyson, Cristian, Ingrid, Baker, Laura, Gripp, Karen, Stessman, Holly A., Eichenberger, Jacob, Jayakar, Parul, Manning, Melanie Ann, Slattery, Leah, Kvarnung, Malin, Kleefstra, Tjitske, de Vries, Bert B.A., Küry, Sébastien, Rosenfeld, Jill A., Meuwissen, Marije E., Vandeweyer, Geert, Kooy, R. Frank

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De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus von Galosi, Serena, Edani, Ban H, Martinelli, Simone, Hansikova, Hana, Eklund, Erik A, Caputi, Caterina, Masuelli, Laura, Corsten-Janssen, Nicole, Srour, Myriam, Oegema, Renske, Bosch, Daniëlle G M, Ellis, Colin A, Amlie-Wolf, Louise, Accogli, Andrea, Atallah, Isis, Averdunk, Luisa, Barañano, Kristin W, Bei, Roberto, Bagnasco, Irene, Brusco, Alfredo, Demarest, Scott, Alaix, Anne-Sophie, Di Bonaventura, Carlo, Distelmaier, Felix, Elmslie, Frances, Gan-Or, Ziv, Good, Jean-Marc, Gripp, Karen, Kamsteeg, Erik-Jan, Macnamara, Ellen, Marcelis, Carlo, Mercier, Noëlle, Peeden, Joseph, Pizzi, Simone, Pannone, Luca, Shinawi, Marwan, Toro, Camilo, Verbeek, Nienke E, Venkateswaran, Sunita, Wheeler, Patricia G, Zdrazilova, Lucie, Zhang, Rong, Zorzi, Giovanna, Guerrini, Renzo, Sessa, William C, Lefeber, Dirk J, Tartaglia, Marco, Hamdan, Fadi F, Grabińska, Kariona A, Leuzzi, Vincenzo

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De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus. Video Material von GALOSI, SERENA, Edani, Ban H., Martinelli, Simone, Hansikova, Hana, Eklund, Erik, Caputi, Caterina, Masuelli, Laura, Corsten-Janssen, Nicole, Srour, Myriam, Oegema, Renske, G. M. Bosch, Daniëlle, Ellis, Colin A., Amlie-Wolf, Louise, Atallah, Isis, Averdunk, Luisa, Barañano, Kristin W., Bei, Roberto, Bagnasco, Irene, Brusco, Alfredo, Demarest, Scott, Alaix, Anne-Sophie, Di Bonaventura, Carlo, Distelmaier, Felix, Elmslie, Frances, Gan-Or, Ziv, Good, Jean-Marc, Gripp, Karen, Kamsteeg, Erik-Jan, Macnamara, Ellen, Marcelis, Carlo, Mercier, Noelle, Peeden, Joseph, Pizzi, Simone, Pannone, Luca, Shinawi, Marwan, Toro, Camilo, E. Verbeek, Nienke, Venkateswaran, Sunita, Wheeler, Patricia G., Zdrazilova, Lucie, Zhang, Rong, Zorzi, Giovanna, Guerrini, Renzo, C. Sessa, William, Lefeber, Dirk, Tartaglia, Marco, Hamdan, Fadi F, Grabinska, Kariona A., Accogli, Andrea

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The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings von Gozes, Illana, Patterson, Marc C, Van Dijck, Anke, Kooy, R Frank, Peeden, Joseph N, Eichenberger, Jacob A, Zawacki-Downing, Angela, Bedrosian-Sermone, Sandra

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Prune perineum von Peeden Jr, Joseph Noble, Wilroy Jr, R. Sidney, Soper, Richard G.

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High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement von Qumsiyeh, Mazin B., Wilroy, R. Sid, Peeden, Joseph N., Tharapel, Avirachan T.

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Reply to Zelante et al von Qumsiyeh, Mazin B., Wilroy, R. Sid, Peeden, Joseph N., Tharapel, Avirachan T.

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Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2 von El-Gharbawy, Areeg H., Peeden Jr, Joseph N., Lachman, Ralph S., Graham Jr, John M., Moore, Stephen R., Rimoin, David L.

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FERTILIZERS CONTAINING ANIMAL NUTRIENT CORE PACKET von MILLER, Joseph M, HOLT, Timothy G, PURSELL, Taylor, PEEDEN, Gregory S, SHIRLEY, JR., Arthur R, COCHRAN, Keith D

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Fertilizers containing animal nutrient core packet von Cochran, Keith D, Peeden, Gregory S, Shirley, Jr., Arthur R, Miller, Joseph M, Pursell, Taylor, Holt, Timothy G

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Fertilizers containing animal nutrient core packet von Cochran, Keith D, Peeden, Gregory S, Shirley, Jr., Arthur R, Miller, Joseph M, Pursell, Taylor, Holt, Timothy G

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FERTILIZERS CONTAINING ANIMAL NUTRIENT CORE PACKET von MILLER, Joseph M, HOLT, Timothy G, PURSELL, Taylor, PEEDEN, Gregory S, SHIRLEY, JR., Arthur R, COCHRAN, Keith D

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FERTILIZERS CONTAINING ANIMAL NUTRIENT CORE PACKET von Miller Joseph M, Cochran Keith D, Holt Timothy G, Pursell Taylor, Peeden Gregory S, Shirley, JR. Arthur R

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