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Deletions and Duplications: A Genetic Variation on Chromosome 16 Associated with Autism -- References

  1. Weiss, L. A., Shen, Y., Korn, J. M., Arking, D. E., Miller, D. T., Fossdal, R., et al. (2008). Association between microdeletion and microduplication at 16p11.2 and autism. The New England journal of medicine, 358(7), 667-75.  View Abstract
  2. Freeman, J. L., Perry, G. H., Feuk, L., Redon, R., McCarroll, S. A., Altshuler, D. M., et al. (2006). Copy number variation: New insights in genome diversity. Genome research, 16(8), 949-961. View Abstract
  3. Redon, R., Ishikawa, S., Fitch, K. R., Feuk, L., Perry, G. H., Andrews, T. D., et al. (2006). Global variation in copy number in the human genome. Nature, 444(7118), 444-454.  View Abstract
  4. Human Genome Structural Variation Working Group, Eichler, E. E., Nickerson, D. A., Altshuler, D., Bowcock, A. M., Brooks, L. D., et al. (2007). Completing the map of human genetic variation. Nature, 447(7141), 161-165.  View Abstract
  5. Lee, J. A., & Lupski, J. R. (2006). Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders. Neuron, 52(1), 103-121.  View Abstract
  6. Lupski, J. R. (2007). Structural variation in the human genome. The New England journal of medicine, 356(11), 1169-1171.  View Abstract
  7. Zhao, X., Leotta, A., Kustanovich, V., Lajonchere, C., Geschwind, D. H., Law, K., et al. (2007). A unified genetic theory for sporadic and inherited autism. Proceedings of the National Academy of Sciences of the United States of America, 104(31), 12831-12836.  View Abstract
  8. Jacquemont, M. L., Sanlaville, D., Redon, R., Raoul, O., Cormier-Daire, V., Lyonnet, S., et al. (2006). Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. Journal of medical genetics, 43(11), 843-849.  View Abstract
  9. Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., et al. (2007). Strong association of de novo copy number mutations with autism. Science (New York, N.Y.), 316(5823), 445-449.  View Abstract
  10. Weiss, L. A., Shen, Y., Korn, J. M., Arking, D. E., Miller, D. T., Fossdal, R., et al. (2008). Association between microdeletion and microduplication at 16p11.2 and autism. The New England journal of medicine, 358(7), 667-75.  View Abstract
  11. Weiss, L. A., Shen, Y., Korn, J. M., Arking, D. E., Miller, D. T., Fossdal, R., et al. (2008). Association between microdeletion and microduplication at 16p11.2 and autism. The New England journal of medicine, 358(7), 667-75.  View Abstract

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on Chromosome 16 Associated with Autism



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