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
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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.
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页码：415 / 419
页数：5
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