Damjanovich Kristy - ARUP Inst Clin & Expt Pathol

Antonie D. Kline,Rick A. Martin,Cherise Klotz, Xiaojing Wang,Rebecca DeSensi,Robin E. Grubs,Bernard J. Costello, Mary L. Marazita, Zahid Ahmad, Elaine H. Zackai, Līvija Medne, Abhimanyu Garg, Valeria Guglielmi, Margaret Adamo, Maria Rosaria D’Apice, Alfonso Bellia, Davide Lauro, Massimo Federici, Renato Lauro, Giuseppe Novelli, Paolo Sbraccia, Adam Shaw,Inge Van Balkom,Mislen Bauer, Trevor Cole, Marie‐Ange Delrue, Arie van Haeringen,Eva Holmberg, Samantha Knight, Geert Mortier, Sheela Nampoothiri,Silvija Pušeljić,Martin Zenker, Valérie Cormier‐Daire, Raoul C. M. Hennekam, James M. Reese,Kimberly A. Aldinger, William B. Dobyns,Karen W. Gripp, Kenneth Lyons Jones, H. Eugene Hoyme,Luther K. Robinson, Miguel del Campo,Melanie A. Manning,Lela M. Prewitt, Christina Chambers,Cecília Mellado, Annapurna Poduri,Danielle Gleason, C Elhosary,Brenda J. Barry,Jennifer N. Partlow, Bernard S. Chang, Gary M. Shaw, A. James Barkovich, Christopher Walsh, Lina Basel‐Vanagaite,Annick Raas-Rotchild, Liora Kornreich,Adi Har‐Zahav, Josefa Yeshaya,Victoria Latarowski, Israela Lerer, Mordechai Shohat, Luitgard Graul‐Neumann,Tina Kienitz, Peter N. Robinson,Sevjidmaa Baasanjav,Benjamin Karow, Gabriele Gillessen‐Kaesbach, Raimund Fahsold, Hartmut Schmidt, Katrin Hoffmann, Eberhard Passarge, Chen Ma, Suzan L. Carmichael, Angela E. Scheuerle, Mark Canfi Eld,Ana Spreiz, Doris Müller,Sibylle Zotter, U. Albrecht, Matthias Baumann,Christine Fauth,Martin Erdel, Johannes Zschocke, Gerd Utermann, Dieter Kotzot, Murat Derbent, Yekta ̈ncel,Kürşad Tokel, Birgül Varan, Ali Haberal, Alper Yazıcı, Eric Legius, Namık ̈zbek, Richard J. Schroer,Kenton R. Holden, Patrick Tarpey, M Matheus, David Griesemer, Michael J. Friez, Jane Fan, Richard J. Simensen, Petter Strømme, Roger E. Stevenson,Michael R. Stratton, Charles E. Schwartz,Ying Fai Ngai,Chieko Chijiwa, Saadet Mercimek‐Mahmutoglu, Laura Stewart,Siu Li Yong, Wendy P. Robinson, William Gibson, Munis Dündar,Aslıhan Kiraz,Şener Taşdemir,Hilal Akalin, Selim Kurtoğlu,Filiz Hafo,Naci Çine,Hakan Savlı,Julie Kaplan, Jonathan A. Bernstein, Alex C. Kwan, Louanne Hudgins,Karen Buysse,Sarah Vergult, Sylvie Mussche,Chantal Ceuterick‐de Groote, Frank Speleman, Björn Menten, Willy Lissens, Rudy Van Coster,J.L. Alessandri, Anna L. David,Dominique Martin–Coignard,J. Ghazouani,Duksha Ramful, Jean‐Louis Laville,C. Le Caignec, Marco Castori, Piero Cascone,Michele Valiante, Luigi Laino, Giorgio Iannetti, Paola Grammatico,Esther Rijntjes-Jacobs, Enrico Lopriore,Sylke J. Steggerda, Sarina G. Kant,Frans J. Walther, Keiko Shimojima, Katsumi Imai, Toshiyuki Yamamoto,Matthew Hand, Colin Gray,Gwen M. Glew,Karen D. Tsuchiya,Piranit Nik Kantaputra, Stefan Mundlos,Warissara Sripathomsawat,Larissa V. Furtado, Pınar Bayrak‐Toydemir,Becki Hulinsky,Kristy Damjanovich, John Carey,Alan F. Rope,Sabine Grønborg,Ralph Krätzner,Juliane Spiegler, Sacha Ferdinandusse, Ronald J. A. Wanders, Hans R. Waterham, Jutta Gärtner,Siham Chafai Elalaoui,Lilia Kraoua, Eline Liger,Ilham Ratbi, Hélène Cavé, Abdelaziz Sefi,Amarilis Sanchez‐Valle, Xueqing Wang, Lorraine Potocki,Zhilian Xia,Sung‐Hae L. Kang, Mattia Carlin,Donnice Michel, Patricia L. Williams,Gerardo Cabrera‐Meza,Ellen K. Brundage,Anna Eifert, Paweł Stankiewicz, Sau Wai Cheung, Seema R. Lalani, Philippe M. Campeau, Leslie Lewis, Shubha R. Phadke, Kerstin Kutsche,Roberta Santos Guilherme, Vilmon de Freitas, A. Meloni, Paulo Roberto Sodré, Denise Maria Christofolini,Renata Pellegrino,Cláudia Berlim de Mello, Laura K. Conlin, Anne Hutchinson, Nancy B. Spinner, Décio Brunoni,Leslie Domenici Kulikowski,Maria Melaragno, Marion Gérard‐Blanluet,Marylin Port‐Lis, Clarisse Baumann,Laurence Perrin‐Sabourin, P Ebrad, G. Audry, Anne‐Lise Delezoide, Alain Verloes

American journal of medical genetics Part Ano. 11 (2010)

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A Novel X‐linked Multiple Congenital Anomaly Syndrome Associated with an EBP Mutation

Larissa V. Furtado,Pinar Bayrak-Toydemir,Becki Hulinsky,Kristy Damjanovich,John C. Carey,Alan F. Rope

American Journal of Medical Genetics Part A（2010）

引用29浏览0WOS引用

P.r672c Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome

Mohammad Al-Haggar,Soheir Yahia,Kristy Damjanovich,Nermin Ahmad,Iman Hamada,Pinar Bayrak-Toydemir

The Indian Journal of Pediatrics（2010）

引用11浏览0WOS引用

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