Výsledky vyhledávání - Sharron Townshend
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Further delineation of the phenotype associated with heterozygous mutations in <i>ZFHX1B</i> Autor Meredith Wilson, David Mowat, Florence Dastot‐Le Moal, Valère Cacheux, Helena Kääriäinen, Danny Cass, Dian Donnai, Jill Clayton‐Smith, Sharron Townshend, Cynthia J. Curry, Michael Gattas, Stephen R. Braddock, Bronwyn Kerr, Salim Aftimos, Harry Zehnwirth, Catherine Barrey, Michel Goossens
Vydáno 2003Artigo -
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Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly–capillary malformation syndrome Autor Laura M. McDonell, Ghayda Mirzaa, Diana Alcantara, Jeremy Schwartzentruber, Melissa T. Carter, Leo J. Lee, Carol L. Clericuzio, John M. Graham, Deborah Morris‐Rosendahl, Tilman Polster, Gyula Acsádi, Sharron Townshend, Simon Williams, Anne Halbert, Bertrand Isidor, Albert David, Christopher D. Smyser, Alex R. Paciorkowski, Marcia Willing, John Woulfe, Soma Das, Chandree L. Beaulieu, Janet Marcadier, Michael T. Geraghty, Brendan J. Frey, Jacek Majewski, Dennis E. Bulman, William B. Dobyns, Mark O’Driscoll, Kym M. Boycott
Vydáno 2013Artigo -
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Targeted prostate cancer screening in men with mutations in <i>BRCA1</i> and <i>BRCA2</i> detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT stud... Autor Anita Mitra, Elizabeth Bancroft, Yolanda Barbáchano, Elizabeth Page, Christopher S. Foster, Charles Jameson, Gillian Mitchell, Geoffrey J. Lindeman, Andrew J. Stapleton, Graeme Suthers, D. Gareth Evans, D. G. Crüger, Ignacio Blanco, Catherine Mercer, Judy Kirk, Lovise Mæhle, Shirley Hodgson, Lyndon Walker, Louise Izatt, Gillian Douglas, Katherine Tucker, Huw Dorkins, Virginia Clowes, Alison Male, Alan Donaldson, C Brewer, Rebecca Doherty, Barbara Bulman, Palle Jørn Sloth Osther, Mónica Salinas, Diana Eccles, Karol Axcrona, Irene Jobson, Barbara Newcombe, Cezary Cybulski, Wendy S. Rubinstein, Saundra S. Buys, Sharron Townshend, Eitan Friedman, Susan M. Domchek, Teresa Ramón y Cajal, Allan D. Spigelman, Soo‐Hwang Teo, Nicola Nicolai, Neil K. Aaronson, Audrey Ardern‐Jones, Chris Bangma, David Dearnaley, Jórunn E. Eyfjörd, Alison Falconer, Henrik Grönberg, Freddie C. Hamdy, Óskar Þór Jóhannsson, Vincent Khoo, Zsofia Kote‐Jarai, Hans Lilja, Jan Lubiński, J Melia, Clare Moynihan, S. Peock, Gad Rennert, Fritz H. Schröder, Paul Sibley, Mohnish Suri, Penny Wilson, Y. J. Bignon, Sara S. Strom, Marc Tischkowitz, Annelie Liljegren, Denisa Ilenčíková, A. Abele, Kyriacos Kyriacou, Christi J. van Asperen, Lambertus A. Kiemeney, Douglas F. Easton, Rosalind A. Eeles
Vydáno 2010Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Microcephaly
Mutation
Pediatrics
Achondroplasia
Agenesis
Agenesis of the corpus callosum
BRCA2 Protein
Cancer
Cancer research
Cell biology
Cognition
Corpus Callosum Agenesis
Corpus callosum
Deubiquitinating enzyme
Differential diagnosis
Disease
Environmental health
Epistemology
Facial dysmorphism
Germline mutation
Hypospadias
Intellectual disability
Internal medicine
Normative
Oncology
PI3K/AKT/mTOR pathway