xxy
英
美
网络 克氏综合征; 小睾丸症; 双性传奇; 性染色体; 我是女生也是男生
双语例句
- 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。 - Objective: To observe the segregation of sex chromosomes in the spermatozoa of a 46, XY/ 47, XXY patient with oligozoospermia.
目的：观察1例46，XY/47，XXY少精子症患者精子性染色体分离的情况。 - Incontinentia pigmenti in a boy with XXY mosaicism detected by fluorescence in situ hybridization
1例荧光原位杂交检测存在XXY镶嵌的男孩出现色素失禁症 - There was no statistical difference between the chromosome XX and XY frequencies in each spermatozoon from the patient in comparison with those estimated in the control.
46，XY/47，XXY少精子症患者与正常对照男性所携带XX精子和XY精子频率比较无统计学差异。 - Case of partial mole was triploid, 69, XXY and with a chromosomal contribution from the female gamete.
1例部分性葡萄胎为三倍体，69，XXY，来源为双精子与一卵子结合而成。文章对完全性葡萄胎和部分性葡萄胎的发生来源做了简要的讨论。 - Results: According to the patients ′ cytogenetics examination, it is found there are 11 cases abnormal chromosomal karyotypes, including 6 cases of chromosome translocation, 2 cases of 47, XXY, 3 cases of big Y chromosome.
结果发现异常核型11例，其中染色体易位6例、2例47，XXY、3例大Y染色体。