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A Bojesen, K Stochholm, S Juul… - Journal of Clinical …, 2011 - Endocrine Soc
Materials and Methods: This was a register study using Danish nationwide registries. One thousand
forty-nine KS men and 100,824 controls were included. Information concerning cohabitation,
fatherhoods, level of education, income, retirement, and death were obtained. Two ...
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A Bojesen… - Acta Paediatrica, 2011 - Wiley Online Library
This is an Accepted Article that has been peer-reviewed and approved for publication in the Acta
Paediatrica, but has yet to undergo copy-editing and proof correction. Please cite this article
as an “Accepted Article”; doi: 10.1111/j.1651-2227.2011.02274.x
Cited by 1 - Related articles - All 3 versions
ME Geffner - Chronic Complex Diseases of Childhood: A …, 2011 - books.google.com
Klinefelter Syndrome Mitchell E. Geffner Klinefelter syndrome is a genetic disorder of males,
caused by the presence of an extra X chromosome, and characterized by small testicles, reduced
testosterone production, and, in most cases, infertility. Etiology Klinefelter syndrome ...
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A Juul, L Aksglaede, K Bay, KM Grigor… - Acta …, 2011 - Wiley Online Library
Sex chromosomes are important for proper sexual differ- entiation. Females carry two X chromosomes
(46,XX), whereas males carry one X chromosome and one Y chro- mosome (46,XY). The SRY
(sex-determining region of Y chromosome) gene is located on the Y chromosome, and ...
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A Ferlin, M Schipilliti, C Vinanzi… - Journal of Clinical …, 2011 - Endocrine Soc
Context: Klinefelter syndrome (KS) is a chromosomal alteration characterized by supernumerary
X-chromosome(s), primary hypogonadism, decreased pubertal peak bone mineral density
(BMD), and accelerated bone loss during adulthood. Decreased bone mass has been ...
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