Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter Syndrome

This publication has 20 references indexed in Scilit:

• Are Adolescent Boys with Klinefelter Syndrome Androgen Deficient? A Longitudinal Study of Finnish 47,XXY Boys
  Pediatric Research, 2006
• Natural history of seminiferous tubule degeneration in Klinefelter syndrome
  Human Reproduction Update, 2005
• Early Androgen Deficiency in Infants and Young Boys with 47,XXY Klinefelter Syndrome
  Hormone Research in Paediatrics, 2005
• Ascertainment Bias in Turner Syndrome: New Insights From Girls Who Were Diagnosed Incidentally in Prenatal Life
  Pediatrics, 2004
• Klinefelter syndrome: Expanding the phenotype and identifying new research directions
  Genetics in Medicine, 2003
• Mental Development in Polysomy X Klinefelter Syndrome (47,XXY; 48,XXXY): Effects of Incomplete X Inactivation
  Seminars in Reproductive Medicine, 2001
• Serum inhibin B levels during male childhood and puberty
  Molecular and Cellular Endocrinology, 2001
• Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
  Nature Genetics, 1997
• Pituitary-Gonadal Function in Klinefelter Syndrome before and during Puberty
  Pediatric Research, 1985
• The XXY (Klinefelter's) syndrome in childhood: Detection and treatment
  The Journal of Pediatrics, 1972