Methodology: Two gene expression data sets of Turner (45,X) and Klinefelter syndrome (47,XXY) were obtained from the Gene Omnibus Expression (GEO) database of the National Center for Biotechnology Information (NCBI). Statistical analysis was performed using R Bioconductor libraries. Differentially ...
来自 NCBI 喜欢 0 阅读量: 55 作者:SH Ong,JR Robertson 摘要: A case of severe schizophrenia is described in a patient with chromosomal mosaicism of Klinefelter's syndrome (XXY) and trisomy 8. The literature of both syndromes is reviewed and the aetiological implications discussed....
NCBI onAcademic 47xxy.ca (全网免费下载) 相似文献 参考文献47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling. 47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosi...
Y chromosome microdeletions in azoospermic patients with Klinefelter's syndrome Aim: To study the occurrence of Y chromosome microdeletions in azoospermic patients with Klinefelter's syndrome (KFS). Methods: Blood and semen samples wer... A Mitra,R Dada,R Kumar,... - 《Asian Journal of And...
万方医学 NCBI NCBI Europe PMC ResearchGate 查看更多 相似文献 引证文献Animal models for Klinefelter's syndrome and their relevance for the clinic In mammals, the contribution of the Y chromosome is paramount for male sexual determination; however, the presence of a single functional X chromosome is ...
Humans Kidney Pregnancy Outcome Karyotyping Klinefelter Syndrome Pregnancy Female Male DOI: 10.1043/1543-2165(2004)1282.0.CO;2 被引量: 10 年份: 2004 收藏 引用 批量引用 报错 分享 全部来源 免费下载 求助全文 全文购买 Semantic Scholar 万方医学 NCBI Europe PMC NCBI 查看更多 相似文献 参考文献 引证...
国家科技图书文献中心 (权威机构) academic.oup.com Europe PMC NCBI NCBI 查看更多 相似文献 参考文献 引证文献Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter's syndrome A retrospective study was carried out in 152 infertile men to determine the prev...
Genotype mosaicism in fragile X fetal tissues The fragile X syndrome is one of the most common familial causes of mental retardation. It is associated with the expression of a fragile site at Xq27.3, a... D, Whrle,MC Hirst,I, Kennerknecht,... 被引量: 0发表: 2019年 ...
We report here a rare case of 47 XXY/46 XY mosaic Klinefelter's syndrome associated with multiple endocrine disorders. A 35-year-old male admitted for the evaluation of renal dysfunction and recurrent bone fractures was diagnosed as having Klinefelter's syndrome by endocrinological examinations and ...
Re: Klinefelter's syndrome XXY.Klinefelter's syndrome is the clinical result of an additional X chromosome in males (47,XXY), although other chromosome abnormalities (such as 46,XY/47,XXY mosaicism; 48,XXXY; 49,XXXXY) account for 10-20% of cases.1 2 ... C Blevins,M Wilson - 《Bmj...