International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences
Author:
Affiliation:
1. The Focus FoundationDavidsonvilleMaryland
2. George Washington UniversityWashingtonDistrict of Columbia
3. Florida International UniversityMiamiFlorida
4. Leiden UniversityRapenburgLeidenNetherlands
Funder
VENI Grant
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38621
Reference38 articles.
1. 47,XXY (KLINEFELTER SYNDROME) AND 47,XYY: ESTIMATED RATES OF AND INDICATION FOR POSTNATAL DIAGNOSIS WITH IMPLICATIONS FOR PRENATAL COUNSELLING
2. The cognitive phenotype in Klinefelter syndrome: A review of the literature including genetic and hormonal factors
3. Prenatal and Postnatal Prevalence of Klinefelter Syndrome: A National Registry Study
4. The Parent-of-Origin of the Extra X Chromosome May Differentially Affect Psychopathology in Klinefelter Syndrome
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2. Klinefelter Syndrome: A Genetic Disorder Leading to Neuroendocrine Modifications and Psychopathological Vulnerabilities in Children—A Literature Review and Case Report;Children;2024-04-24
3. Reading skills in males with 47,XXY: Risk factors and the influence of hormonal replacement therapy (HRT);Genetics in Medicine;2023-08
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5. Structural and pragmatic language in young children with sex chromosome trisomy (XXX, XXY, XYY): Predictive value for neurobehavioral problems one year later;The Clinical Neuropsychologist;2022-04-28
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