一名患有尾部退化异常的婴儿体内的一条双随体标记染色体。
A bisatellited marker chromosome in an infant with the caudal regression anomalad.
作者信息
Jensen P K, Hansen P
出版信息
Clin Genet. 1981 Feb;19(2):126-9. doi: 10.1111/j.1399-0004.1981.tb00682.x.
Abstract
An infant with the caudal regression anomalad is described. Karyotypic analysis revealed mosaicism for a bisatellited microchromosome. Using banding techniques, an attempt was made to further identify the marker chromosome. It is suggested that a causal relationship exists between the cytogenetic findings and the clinical observations.
摘要
本文描述了一名患有尾椎退化异常的婴儿。核型分析显示存在一条双随体微小染色体的嵌合体。运用显带技术，尝试进一步鉴定这条标记染色体。提示细胞遗传学发现与临床观察之间存在因果关系。
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