All Stories

  1. International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences

    Article • American Journal of Medical Genetics Part A, February 2018, Wiley

    Dr Carole Samango-Sprouse

  2. The benefits and limitations of cell-free DNA screening for 47, XXY (Klinefelter syndrome)

    Article • Prenatal Diagnosis, April 2017, Wiley

    Dr Carole Samango-Sprouse

  3. 10-year-old female with intragenic KANSL1 mutation, no KANSL1 -related intellectual disability, and preserved verbal intelligence

    Article • American Journal of Medical Genetics Part A, February 2017, Wiley

    Dr Carole Samango-Sprouse

  4. Expanding the phenotypic profile of Kleefstra syndrome: A female with low-average intelligence and childhood apraxia of speech

    Article • American Journal of Medical Genetics Part A, February 2016, Wiley

    Dr Carole Samango-Sprouse

  5. Expanding the phenotypic profile of boys with 47, XXY: The impact of familial learning disabilities

    Article • American Journal of Medical Genetics Part A, April 2014, Wiley

    Dr Carole Samango-Sprouse