Novel genetic aspects of Klinefelter's syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine
Link
http://academic.oup.com/molehr/article-pdf/16/6/386/6414856/gaq019.pdf
Reference117 articles.
1. Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter’s syndrome
2. 47,XXY (KLINEFELTER SYNDROME) AND 47,XYY: ESTIMATED RATES OF AND INDICATION FOR POSTNATAL DIAGNOSIS WITH IMPLICATIONS FOR PRENATAL COUNSELLING
3. Trisomy of the short stature homeobox-containing gene (SHOX ), resulting from a duplication-deletion of the X chromosome
4. Natural history of seminiferous tubule degeneration in Klinefelter syndrome
5. Abnormal Sex Chromosome Constitution and Longitudinal Growth: Serum Levels of Insulin-Like Growth Factor (IGF)-I, IGF Binding Protein-3, Luteinizing Hormone, and Testosterone in 109 Males with 47,XXY, 47,XYY, or Sex-Determining Region of the Y Chromosome (SRY)-Positive 46,XX Karyotypes
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