检索结果 - William Allen
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Artificial Intelligence-Driven Analysis Identifies Anterior Cruciate Ligament Reconstruction, Hip Arthroscopy and Femoroacetabular Impingement Syndrome, and Shoulder Instability as... 由 Henry B. G. Baird, William Allen, María‐Trinidad Gallegos, Cody Ashy, Harris S. Slone, W. Michael Pullen
出版 2025Revisão -
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Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures 由 Stephen R. Williams, Sureni V. Mullegama, Jill A. Rosenfeld, Aditi I Dagli, Eli Hatchwell, William Allen, Charles A. Williams, Sarah H. Elsea
出版 2009Artigo -
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Loss-of-function mutations in the human <i>GLI2</i> gene are associated with pituitary anomalies and holoprosencephaly-like features 由 Erich Roessler, Yangzhu Du, José L. Mullor, Esther Casas, William Allen, Gabriele Gillessen‐Kaesbach, Elizabeth Roeder, Jeffrey E. Ming, Ariel Ruiz i Altaba, Maximilian Muenke
出版 2003Artigo -
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HOW TO MAKE A DOCTOR: AN UNUSUAL SYMPOSIUM ON THE ESSENTIALS OF MEDICAL EDUCATION 由 Wilbur, Ray Lyman, Pusey, William Allen, Strickler, David A., Colwell, N. P., Zapffe, Frederick C., Rodman, J. S., Ophuls, William, Schmitt, L. S., Phillips, Percy T., Magan, Percy T., Musgrave, William Everett
出版 1925Text -
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NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease 由 Paige Martin, Yu Kigoshi-Tansho, Roger B. Sher, Gianina Ravenscroft, Jennifer E. Stauffer, Rajesh Kumar, Ryo Yonashiro, Tina Müller, Christopher Griffith, William Allen, Davut Pehli̇van, Tamar Harel, Martin Zenker, Denise Howting, Denny Schanze, Eissa Faqeih, Naif A. M. Almontashiri, Reza Maroofian, Henry Houlden, Neda Mazaheri, Hamid Galehdari, Ganka Douglas, Jennifer E. Posey, Monique M. Ryan, James R. Lupski, Nigel G. Laing, Claudio A.P. Joazeiro, Gregory A. Cox
出版 2020Artigo -
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Comparing Outcomes with Bone Marrow or Peripheral Blood Stem Cells as Graft Source for Matched Sibling Transplants in Severe Aplastic Anemia across Different Economic Regions 由 Kumar, Rajat, Kimura, Fumihiko, Ahn, Kwang Woo, Hu, Zhen-Huan, Kuwatsuka, Yachiyo, Klein, John P., Pasquini, Marcelo, Miyamura, Koichi, Kato, Koji, Yoshimi, Ayami, Inamoto, Yoshihiro, Ichinohe, Tatsuo, Wood, William Allen, Wirk, Baldeep, Seftel, Matthew, Rowlings, Philip, Marks, David I, Schultz, Kirk R., Gupta, Vikas, Dedeken, Laurence, George, Biju, Cahn, Jean-Yves, Szer, Jeff, Lee, Jong Wook, Ho, Aloysius YL, Fasth, Anders, Hahn, Theresa, Khera, Nandita, Dalal, Jignesh, Bonfim, Carmem, Aljurf, Mahmoud, Atsuta, Yoshiko, Saber, Wael
出版 2016Text -
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De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies 由 Konrad Platzer, Heinrich Sticht, Stacey L. Edwards, William Allen, Kaitlin M. Angione, Maria Teresa Bonati, Campbell K. Brasington, Megan T. Cho, Laurie Demmer, Tzipora C. Falik‐Zaccai, Candace Gamble, Yorck Hellenbroich, Maria Iascone, Fernando Kok, Sonal Mahida, Hanna Mandel, Thorsten Marquardt, Kirsty McWalter, Bianca Panis, Alexander Pepler, Hailey Pinz, Luiza Ramos, Deepali N. Shinde, Constance Smith‐Hicks, Alexander P.A. Stegmann, Petra Stöbe, Constance T. R. M. Stumpel, Carolyn M. Wilson, Johannes R. Lemke, Nataliya Di Donato, Kenneth G. Miller, Rami Abou Jamra
出版 2019Artigo -
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Scoring System Prognostic of Outcome in Patients Undergoing Allogeneic Hematopoietic Cell Transplantation for Myelodysplastic Syndrome 由 Shaffer, Brian C., Ahn, Kwang Woo, Hu, Zhen-Huan, Nishihori, Taiga, Malone, Adriana K., Valcárcel, David, Grunwald, Michael R., Bacher, Ulrike, Hamilton, Betty, Kharfan-Dabaja, Mohamed A., Saad, Ayman, Cutler, Corey, Warlick, Erica, Reshef, Ran, Wirk, Baldeep Mona, Sabloff, Mitchell, Fasan, Omotayo, Gerds, Aaron, Marks, David, Olsson, Richard, Wood, William Allen, Costa, Luciano J., Miller, Alan M., Cortes, Jorge, Daly, Andrew, Kindwall-Keller, Tamila L., Kamble, Rammurti, Rizzieri, David A., Cahn, Jean-Yves, Gale, Robert Peter, William, Basem, Litzow, Mark, Wiernik, Peter H., Liesveld, Jane, Savani, Bipin N., Vij, Ravi, Ustun, Celalettin, Copelan, Edward, Popat, Uday, Kalaycio, Matt, Maziarz, Richard, Alyea, Edwin, Sobecks, Ron, Pavletic, Steven, Tallman, Martin, Saber, Wael
出版 2016Text -
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Mutations in TOP3A Cause a Bloom Syndrome-like Disorder 由 Carol-Anne Martin, Kata Sarlós, Clare V. Logan, Roshan Singh Thakur, David Parry, Anna H. Bizard, Andrea Leitch, Louise Cleal, Nadia Shaukat Ali, Mohammed Al‐Owain, William Allen, Janine Altmüller, Miriam Aza‐Carmona, Bushra A.Y. Barakat, Jimena Barraza‐García, Amber Begtrup, Massimo Bogliolo, Megan T. Cho, Jaime Cruz‐Rojo, Hassan Ali Mundi Dhahrabi, Nursel Elçioğlu, Gráinne S. Gorman, Rebekah Jobling, Ian Kesterton, Yoshihito Kishita, Masakazu Kohda, Polona Le Quesne Stabej, Asam Jassim Malallah, Peter Nürnberg, Akira Ohtake, Yasushi Okazaki, Roser Pujol, Marı́a José Ramı́rez, Anya Revah‐Politi, Masaru Shimura, Paul E. Stevens, Robert W. Taylor, Lesley Turner, Hywel Williams, Carolyn M. Wilson, Gökhan Yigit, Laura Zahavich, Fowzan S. Alkuraya, Jordi Surrallés, Alejandro Iglesias, Kei Murayama, Bernd Wollnik, Mehul Dattani, Karen E. Heath, Ian D. Hickson, Andrew P. Jackson
出版 2018Artigo
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