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MARKER AND KIT FOR DIAGNOSING CHROMOSOMAL ABNORMALITY OF NEUROBLASTOMA THROUGH MICROARRAY
MARKER AND KIT FOR DIAGNOSING CHROMOSOMAL ABNORMALITY OF NEUROBLASTOMA THROUGH MICROARRAY
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机译:通过微阵列诊断神经母细胞瘤染色体异常的标记物和试剂盒
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摘要
PURPOSE: A kit and method for diagnosing chromosomal abnormality of novel neuroblastoma are provide to accurately measure the loss of chromosome through BAC(bacterial artificial chromosome) array.;CONSTITUTION: A CGH(comparative genomic hybridization) for diagnosing neuroblastoma comprises: a human second chromosome p25.3-p16.3 part which is able to confirm gain of chromosome by the increase of the number of DNA copies; a human seventh chromosome entire part which is able to confirm chromosome gain by increase of the number of DNA copies; a human 14th chromosome which is able to confirm chromosome deletion by reduction of the number of DNA copies and a human 22th chromosome q13.1-q13.2 part which is able to confirm chromosome deletion by reduction of the number of DNA copies.;COPYRIGHT KIPO 2010
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