Patients with Klinefelter's syndrome are generally characterized by a 47, XXY karyotype, seminiferous tubule dysgenesis, azoospermia and infertility. Klinefelter综合征患者以47,XXY核型,睾丸精曲小管发育不良,无精子症和不育为特征。
The clinical signs of ninety-one patients with classical 47, XXY Klinefelter's syndrome met with were reviewed. 总结1974~1991年间91例47,XXY克氏综合征的临床体征,发现腋毛和胡须减少或消失,下体长,以及小而软的睾丸是本病的重要体征。
Clinical genetics studies of 40 patients with klinefelter's syndrome 40例Klinefelter综合征的临床遗传学研究
Study on pituitary-gonadal function in patients with klinefelter's syndrome Klinefelter氏综合征患者垂体-性腺内分泌功能研究
Effect of testosterone undecanoate on the function of pituitary testis axis in the patients with Klinefelter's syndrome 十一酸睾酮对Klinefelter综合征患者垂体性腺轴系功能的影响
Klinefelter's Syndrome ( A Case Report) Klinefelter氏综合征(附病例报告)
Objective: To analysis the aneuploidy rate of X, Y and 18 chromosomes of sperms from a patient of Klinefelter's syndrome and to guide the assisted reproductive treatment. 目的分析Klinefelter综合征病人精子X,Y,18染色体的非整倍体率(aneuploid),指导其辅助生育治疗。
Objective: To study the variation of X chromosome centromeric Alpha Satellite DNA in Klinefelter's syndrome patients, their parents and normal individuals and to discuss the mechanism of Klinefelter's syndrome X chromosome nondisjunction. 目的:本文从DNA分子水平对Klinifelter综合征患者及双亲X染色体着丝粒区域的α-卫星DNA变异进行研究,探讨Klinefelter综合征患者X染色体不分离形成的原因。
X chromosome centromeric alpha satellite DNA variation in Klinefelter's syndrome patients and their parents Klinefelter综合征及双亲X染色体着丝粒区α-卫星DNA变异研究
The Measurement on Base Value of 9 Serum Hormones in Klinefelter's Syndrome Klinefelter's综合征患者9项血清激素基础值的测定
Acute pulmonary thromboembolism associated with Klinefelter's syndrome: the first case report and review of the literature in china 先天性睾丸发育不全综合征并发肺血栓栓塞症1例并文献复习