Author:
Radicioni A. F.,Ferlin A.,Balercia G.,Pasquali D.,Vignozzi L.,Maggi M.,Foresta C.,Lenzi A.
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference148 articles.
1. Klinefelter HF, Reifenstein EC, Albright F. Syndrome characterized by gynecomastia, aspermatogenesis without a leydigism and increased excretion of follicle-stimulating hormone. J Clin Endocrinol Metab 1942, 2: 615–27.
2. Jacobs PA, Strong JA. A case of Human intersexuality having a possible XXY sex-determining mechanism. Nature 1959, 183: 302–3.
3. Bojesen A, Juul S, Gravholt CH. Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J Clin Endocrinol Metab 2003, 88: 622–6.
4. Abramsky L, Chappie J. 47, XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counseling. Prenat Diagn 1997, 17: 363–68.
5. Nielsen J, Wohlert M. Sex chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Birth Defects Orig Artic Ser 1990, 26: 209–23.
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