13号染色体短臂增多核型的产前诊断
Prenatal diagnosis of a 13p+ karyotype.
作者信息
Soudek D
出版信息
Hum Genet. 1979 Oct 2;51(3):339-41. doi: 10.1007/BF00283406.
PMID:511167
Abstract
Chromosome 13p+ was identified in an amniotic cell culture. The variant has been inherited for three generations without adverse effect.
摘要
在羊水细胞培养中发现了13号染色体短臂增加。该变异已遗传三代，无不良影响。
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