Klinefelter Syndrome (KS): Scientific Articles

Featured Articles

The following featured articles include those from NICHD researchers or NICHD-supported researchers.

  • Visootsak, J., Ayari, N., Howell, S., Lazarus, J., & Tartaglia, N. (2013). Timing of diagnosis of 47,XXY and 48,XXYY: A survey of parent experiences. American Journal of Medical Genetics Series A, 161A(2), 268-272. PMID: 23322622
  • Bryant, D. M., Hoeft, F., Lai, S., Lackey, J., Roeltgen, D., Ross, J., & Reiss, A. L. (2012). Sex chromosomes and the brain: A study of neuroanatomy in XYY syndrome. Developmental Medicine and Child Neurology, 54(12), 1149-1156. PMID: 23057627
  • Bryant, D. M., Hoeft, F., Lai, S., Lackey, J., Roeltgen, D., Ross, J., et al. (2011). Neuroanatomical phenotype of Klinefelter syndrome in childhood: A voxel-based morphometry study. Journal of Neuroscience, 31(18), 6654-6660. PMID: 21543594
  • Tartaglia, N., Cordeiro, L., Howell, S, Wilson, R., & Janusz, J. (2010). The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome). Pediatric Endocrinology Reviews, 8 Suppl 1, 151-159. PMID: 21217607
  • Yatsenko, A. N., Yatsenko, S. A., Weedin, J. W., Lawrence, A. E., Patel, A., Peacock, S., et al. (2010). Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men. Journal of Urology, 183(4),1636-1642. PMID: 20172548
  • Visootsak, J., & Graham, J. M. Jr. (2009). Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY. Developmental Disabilities Research Reviews, 15(4), 328-332. PMID: 20014367
  • Steinman, K., Ross, J., Lai, S., Reiss, A., & Hoeft, F. (2009). Structural and functional neuroimaging in Klinefelter (47,XXY) syndrome: A review of the literature and preliminary results from a functional magnetic resonance imaging study of language. Developmental Disabilities Research Review, 15(4):295-308. PMID: 20014370

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