Výsledky vyhledávání - Kath Smith
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1
Cellular differentiation hierarchies in normal and culture-adapted human embryonic stem cells Autor Tariq Enver, Shamit Soneji, Chirag Joshi, John Brown, Francisco J. Iborra, Torben Ørntoft, Thomas Thykjær, Edna L. Maltby, Kath Smith, Raed Abu Dawud, Mark Jones, Maryam Moghaddam Matin, Paul J. Gokhale, Jonathan S. Draper, Peter W. Andrews
Vydáno 2005Artigo -
2
Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype Autor Meena Balasubramanian, Kath Smith, Lina Basel‐Vanagaite, Murray Feingold, Pamela Brock, Gordon C. Gowans, Pradeep Vasudevan, Lara Cresswell, Emma‐Jane Taylor, Civonnia Harris, Neil Friedman, Rocio Moran, Holly Feret, Elaine H. Zackai, Aaron Theisen, Jill A. Rosenfeld, Michael Parker
Vydáno 2011Artigo -
3
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome Autor Bregje W.M. van Bon, Heather C. Mefford, Björn Menten, David A. Koolen, Andrew J. Sharp, Willy M. Nillesen, Jeffrey W. Innis, Thomy de Ravel, Catherine L. Mercer, Marco Fichera, Helen Stewart, Louise Connell, Katrin Õunap, Katherine Lachlan, B. Castle, Nathalie Van der Aa, Conny van Ravenswaaij, Marcelo A. Nóbrega, Clara Serra‐Juhé, Ingrid Simonic, Nicole de Leeuw, Rolph Pfundt, Ernie M.H.F. Bongers, Carl Baker, P Finnemore, Shuwen Huang, V. Maloney, John A. Crolla, M van Kalmthout, Maurizio Elia, Geert Vandeweyer, J. P. Fryns, Sandra Janssens, Nicola Foulds, S Reitano, Kath Smith, Sven Parkel, Bart Loeys, C. Geoffrey Woods, Anna Oostra, Frank Speleman, Alexandre C. Pereira, Ants Kurg, Lionel Willatt, Samantha J.L. Knight, Joris Vermeesch, Corrado Romano, John Barber, Geert Mortier, Luis Alberto Pérez‐Jurado, R. Frank Kooy, Han G. Brunner, Evan E. Eichler, Tjitske Kleefstra, Bert B.A. de Vries
Vydáno 2009Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Phenotype
Bioinformatics
Cell biology
Cellular differentiation
Clinical significance
Computational biology
Copy-number variation
Embryonic stem cell
Epilepsy
Evolutionary biology
Gene duplication
Genome
Haploinsufficiency
Internal medicine
Microdeletion syndrome
Mutation
Proband
Psychiatry
Stem cell