The last step in developing this demo XUL application is to make the controls work.

1、

Develop Rich Client Web Application Based on XUL

基于XUL开发富客户端应用程序

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2、

This is simple XUL code to create a search form.

这是一段简单的XUL代码，可创建一个搜索表单。

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3、

The Extending of Optical Films to XUV Region

光学薄膜向XUV区的扩展

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4、

The XUV spectra of laser-produced Ag plasma

激光银等离子体XUV谱测量

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5、

The development of the generation of coherent VUV/ XUV radiation by nonlinear optical process

非线性光学产生VUV/XUV相干辐射的发展和研究

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6、

Aluminum Grating Target Used in XUV Radiograph System

用于X光成像系统像传递函数的Al静态成像靶

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7、

Aluminium XUV spectra excited in a line focus laser& produced plasma

线聚焦激光辐照Al靶所产生的紫外X射线谱线

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8、

Silicon grating foil used to analyze the image transfer function in XUV radiography system

XUV成像系统中像传递函数研究用的Si刻蚀膜

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9、

A stigmatic grazing incidence grating spectrograph and laser plasma XUV emission spectra

消像散掠入射光栅光谱仪和激光等离子体极紫外发射光谱

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10、

Then were big Y chromosome, four cases, accounting for 7.02% of patients studied and 17.39% of those with ACK: 46, XY/ 47, XXY and 47, XXY, one case for each type.

其次为大Y染色体4例，检出率为7.02%，占异常核型的7.39%。46，XY/47，XXY和47，XYY各1例，检出率为1.75%，占异常核型的4.35%。

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11、

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。

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12、

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。

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13、

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。

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14、

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。

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15、

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

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16、

A 45, X/ 47, XYY Mosaicism in a Phenotypic Female Hermaphrodite

核型45，X/47，XYY嵌合体女性表型一例报告

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17、

Xyy syndrome and behavioral abnormality

XYY综合征与行为异常

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18、

13; 22 translocation type of 22 trisomy and 15; y translocation type of XYY karyotype& case Report

13；22易位型22三体征及15；Y易位型XYY核型各一例报告

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19、

The aspects of main researched have: 1, ascertain the color area of the CIE xyY color space.

主要研究的方面有：1、CIE xyY颜色空间的色域确定。

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20、

A Molecular Analysis of Females with 46, XY or 47, XYY Karyotype

46，XY女性和47，XYY女性的分子遗传学分析

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