由新发9/15易位和9号染色体短臂等臂染色体导致的9号染色体短臂三体。
Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.
作者信息
Sandig K R, Mücke J, Veit H
出版信息
Hum Genet. 1979 Nov;52(2):175-8. doi: 10.1007/BF00271570.
PMID:511173
Abstract
Trisomy 9p with de novo 9/15 translocation and 9p isochromosome was observed in a mentally defective boy with typical clinical features for this syndrome. This chromosomal aberration is probably caused by the pericentric inversion of chromosome 9 of the patient's father.
摘要
在一名患有该综合征典型临床特征的智力缺陷男孩中观察到9号染色体短臂三体伴新发9/15易位和9号染色体短臂等臂染色体。这种染色体畸变可能是由患者父亲9号染色体的臂间倒位引起的。
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