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- normal male infant 正常男婴
- A 35-day-old male infant was scheduled for bilateral inguinal herniorrhaphy. 摘要一个三十五天大的幼儿接受二沟腹股沟疝气门诊手术。
- Peripheral blood cyto genetic study revealed a normal male karyotype. 周边血液细胞遗传学检查显示为正常男性染色体核型。
- The first patient, a male infant, presented with abdominal distention and vomiting for two days at the age of four months. 首位四个月的男性病婴,以腹胀及持续呕吐表现,另一个九个月大男婴则以发烧一日、躁动不安,喂食后呕吐及喜作左侧躺表现。
- In the present study, a male infant developed focal seizure and intracranial hemorrhage without cardiac decompensation at the age of 42 days. 电脑断层检查和血管摄影显示:病人脑内有广泛,对称性的钙化,并且在左顶叶有一动静瘘管。
- Methods 58 lumbar segments of the LTV collected from normal male cadavers were grouped according to their diameters. 统计学分析表明,左睾丸静脉管径与瓣膜出现率以及末端开口瓣膜出现率之间不存在相关关系。
- Factors associated with poor postpartum sleep quality were depression, history of sleep problems, primiparity, not exclusively breast-feeding, or having a younger or male infant. 与产后睡眠品质不佳有关的因素包括忧郁、曾有睡眠问题、初产妇、未完全哺喂母奶、家有幼童或者生的是男婴。
- Methods:Thirty-five cases of BPH and twenty normal male adults (as control) were studied by urodynamic method. 方法:对20例正常成人和35例BPH患者进行尿流动力学研究。
- Karyotyping for adanced maternal age was performed by amniocentesis and demonstrated a normal male karyotype (46 XY with G-banding). 对此高龄孕妇行羊膜穿刺染色体组型分型检查,先是正常男性(46XY,G带显带技术)。
- We present a case of multicentric infantile myofibromatosis in a 3-month-old male infant who had multiple papular lesions on his extremities and trunk and a slowly growing and bulging mass on his left occipital area since birth. 摘要我们报告一例多中心性婴儿肌纤维瘤病于一位三个月大的男婴,在出生后发现下肢与躯干有数个丘疹样病灶,同时于左枕骨部也发现了一个膨出且缓慢变大的肿块。
- Furthermore, in order to validate the results of the finite element analysis, the plantar pressures of five normal male subjects’ left foot were obtained. 此外,亦分别进行五位正常男性左足之足底压力量测实验十次,比较模拟分析与实验之结果,作为有限元素分析结果之验证。
- Using biotinylated human Y-specificDNA probe PHY2.1 and Cos 84, we carriedout Southern and dot hybridization withhuman DNA from artificially aborted cho-rionic villi. and with DNA of peripherallymphocytes from normal male and female. 作者以流产绒毛和外周血淋巴细胞DNA为材料;通过Southern印迹杂交和点杂交;考察了用生物素标记Y特异DNA探针PHY2.;1和Cos84进行产前性别诊断的可行性。
- Results The single lymphocyte amplification rates of Amelogenin, DXS15, F8Civs13 and DXS1073 were 94.29%, 91.43%, 100% and 100% in a normal male, and 100%, 97.14%, 97.14% and 97.14% in a normal female. Amelogenin、DXS15、F8Civs13和DXS1073在男性的单细胞扩增成功率分别为94.;29%25、91
- Methods:We detected normal male and Duchenne muscular dystrophy patients with detetion in exon 48 or 51 by using in situ PCR to amplify exon 48 or 51.Results:Most of normal male (96%) showed signal spots in lymphocyte,but the patients had no spots. 方法 :应用抗肌萎缩蛋白 (dystrophin)的基因 48及 5 1号外显子的引物 ,使用直接法原位PCR ,检测正常人及Duchenne型肌营养不良症 (DMD)患者。 结果 :正常男性 96%25间期淋巴细胞出现信号斑点 ,而DMD缺失型患者间期淋巴细胞均未出现信号斑点。
- Objective:To analyze G6PD gene mutation in 168 Cantonese G6PD deficient male infants. 目的:对168例广东籍男婴葡萄糖-6-磷酸脱氢酶(G6PD)缺陷者进行G6PD基因突变型研究。
- Radioimmune assay was applied to determine EGP, LH, FSH and T values among 73 infertile males and 39 normal males. 用放免法测定73例不育男性和39例正常对照EGP、LH、FSH、T水平。
- Male infants, young boys and adult men may have a variety of problems affecting their physical appearance, their sex organs, or their sexual responses. 男婴、少年和成年男子可能有著影响他们生理外貌、性器官或性反应的各种各样的病症。
- Methods 30 cases (16 males and 14 females) of AION at the papilloedema stage were examined and compared with the control group including 16 normal males and 14 normal females. 方法缺血性视乳头病变患者30例(男16例,女14例)与30例可以与之匹配的健康人进行对照(男16例,女14例),进行血液流变学检查及统计学处理。
- The computer has a normal qwerty keyboard. 这台计算机有标准的英文键盘。
- The situation has returned to normal in the city. 这座城市的局势已恢复正常。