نتائج البحث - Alice Bailey
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Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS حسب Donna M. McDonald‐McGinn, Somayyeh Fahiminiya, Timothée Revil, Beata Nowakowska, Joshua A. Suhl, Alice Bailey, Elisabeth E. Mlynarski, David R. Lynch, Albert C. Yan, Larissa T. Bilaniuk, Kathleen E. Sullivan, Stephen T. Warren, Beverly S. Emanuel, Joris Vermeesch, Elaine H. Zackai, Loydie A. Jerome‐Majewska
منشور في 2012Artigo -
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What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia حسب Ian M. Campbell, Sarah E. Sheppard, T. Blaine Crowley, Daniel E. McGinn, Alice Bailey, Michael J. McGinn, Marta Unolt, Jelle F. Homans, Erin Chen, Harold I. Salmons, J. William Gaynor, Elizabeth Goldmuntz, Oksana A. Jackson, Lorraine E. Levitt Katz, Maria R. Mascarenhas, Vincent F. Deeney, René M. Castelein, Karen B. Zur, Lisa M. Elden, Staci Kallish, Thomas F. Kolon, Sarah Hopkins, Madeline Chadehumbe, Michele P. Lambert, Brian J. Forbes, Julie S. Moldenhauer, Erica Schindewolf, Cynthia Solot, Edward Moss, Raquel E. Gur, Kathleen E. Sullivan, Beverly S. Emanuel, Elaine H. Zackai, Donna M. McDonald‐McGinn
منشور في 2018Artigo -
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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes حسب Maria Delio, Tingwei Guo, Donna M. McDonald‐McGinn, Elaine H. Zackai, Sean Herman, Mark Kaminetzky, Anne Marie Higgins, Karlene Coleman, Carolyn Chow, Maria Jarlbrzkowski, Carrie E. Bearden, Alice Bailey, Anders Vangkilde, Line Olsen, Charlotte Olesen, Flemming Skovby, Thomas Werge, Ludivine Templin, Tiffany Busa, Nicole Philip, Ann Swillen, Joris Vermeesch, Koenraad Devriendt, Maude Schneider, Sophie Dahoun, Stéphan Eliez, Kelly Schoch, Stephen R. Hooper, Vandana Shashi, Joy Samanich, Robert Marion, Thérèse van Amelsvoort, Erik Boot, Petra Klaassen, Sasja N. Duijff, Jacob Vorstman, Tracy Yuen, Candice K. Silversides, Eva W.C. Chow, Anne S. Bassett, Amos Frisch, Abraham Weizman, Doron Gothelf, Maria Niarchou, Marianne B. M. van den Bree, Michael J. Owen, Damián Heine‐Suñer, Jordi Rosell Andreo, Marco Armando, Stefano Vicari, Maria Cristina Digilio, Adam Auton, Wendy R. Kates, Tao Wang, Robert J. Shprintzen, Beverly S. Emanuel, Bernice E. Morrow
منشور في 2013Artigo
أدوات البحث:
موضوعات ذات صلة
Medicine
Biology
DiGeorge syndrome
Gene
Genetics
Internal medicine
Biopsy
Breast cancer
Cancer
Cohort
Deletion syndrome
Disease
Environmental health
Gamma probe
Genetic recombination
Homologous chromosome
Lymph node
Meiosis
Mutation
Node (physics)
Non-allelic homologous recombination
Nuclear medicine
Pathology
Pediatrics
Phenotype
Physics
Population
Proband
Psychiatry
Quantum mechanics