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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 30, 2013
Prenatal diagnosis and 47,XXYJoe Leigh Simpson, Carole Samango-SprousePediatric Endocrinology Reviews : PER|January 11, 2011
Expansion of the phenotypic profile of the young child with XXYCarole Samango-SprousePrenatal Diagnosis|March 28, 2017
The benefits and limitations of cell-free DNA screening for 47, XXY (Klinefelter syndrome)Carole Samango-Sprouse, Colleen Keen, Teresa Sadeghin, et al.American Journal of Medical Genetics. Part A|February 18, 2017
10-year-old female with intragenic KANSL1 mutation, no KANSL1-related intellectual disability, and preserved verbal intelligenceColleen Keen, Carole Samango-Sprouse, Holly Dubbs, et al.Frontiers in Endocrinology|December 12, 2025
Incidence of miscarriages in women with children with 47,XXY, 48,XXXY, or 49,XXXXYElizabeth Moser, Margaret Olaya, Andrea Gropman, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 25, 2013
Immunodeficiency in patients with 49,XXXXY chromosomal variationMichael D Keller, Teresa Sadeghin, Carole Samango-Sprouse, et al.American Journal of Medical Genetics. Part A|January 15, 2019
The incidence of anxiety symptoms in boys with 47,XXY (Klinefelter syndrome) and the possible impact of timing of diagnosis and hormonal replacement therapyCarole Samango-Sprouse, Patricia Lasutschinkow, Sherida Powell, et al.American Journal of Medical Genetics. Part A|June 19, 2015
Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXXCarole Samango-Sprouse, Colleen Keen, Francie Mitchell, et al.Annals of the New York Academy of Sciences|June 25, 2008
Genetic and phenotypic heterogeneity in ovarian failure: overview of selected candidate genesJoe Leigh SimpsonPageof 13