References
Aiyar, R. S., J. Gagneur, and L. M. Steinmetz. (2008) “Identification of Mitochondrial Disease Genes Through Integrative Analysis of Multiple Datasets.” Methods 46: 248–255.
Alderton, G. K., H. Joenje, R. Varon, A. D. Borglum, P. A. Jeggo, and M. O’Driscoll. (2004) “Seckel Syndrome Exhibits Cellular Features Demonstrating Defects in the ATR-Signalling Pathway.” Human Molecular Genetics 13: 3,127–3,138.
Allouche, M. (2007) “ALK Is a Novel Dependence Receptor: Potential Implications in Development and Cancer.” Cell Cycle 6: 1,533–1,538.
Amir, R. E., I. B. Van den Veyver, M. Wan, C. Q. Tran, U. Francke, and H. Y. Zoghbi. (1999) “Rett Syndrome Is Caused by Mutations in X-Linked MECP2, Encoding Methyl-CpG-Binding Protein 2.” Nature ...
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