Chromosome analysis in brother cases of Kallmann's syndrome by using fluorescence in situ hybridization, comparative genomic hybridization, multicolor spectral karyotyping

被引：0

作者：

Kobayashi, T ^{[1
]}

Joe, Y ^{[1
]}

Tokunaga, Y ^{[1
]}

Morioka, M ^{[1
]}

Tanaka, H ^{[1
]}

机构：

[1] Kawasaki Med Sch, Dept Urol, Kurashiki, Okayama, Japan

来源：

ANDROLOGY IN THE 21ST CENTURY, SHORT COMMUNICATIONS | 2001年

关键词：

D O I：

暂无

中图分类号：

R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

摘要：

We reported Kallmann's syndrome in brother cases with chromosome analysis using by fluorescence in situ hybridization (FISH), comparative genomic hybridization (CGH), multicolor karyotyping (M-FISH). KAL gene existed on Xp22.3 of two cases in FISH analysis. In CGH analysis, some new chromosome aberrations were as gain of Xq12., Yq11, Yp11.3. and loss of 9p21-24. In M-FISH analysis, We couldn't find out translocation and deletion on whole chromosome of two cases.

引用

页码：415 / 419

页数：5

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