由于家族性易位，8p21三体导致短臂缺失。
Trisomy for 8p21 leads to pter owing to a familial translocation.
作者信息
Allen E F, Hodgkin W E
出版信息
J Med Genet. 1983 Feb;20(1):68-9. doi: 10.1136/jmg.20.1.68.
Abstract
A girl with developmental delay and physical abnormalities was trisomic for the segment 8p21→pter owing to a familial translocation t(8;11). The child's father and paternal grandmother carry the same translocation.
摘要
一名患有发育迟缓及身体异常的女孩因家族性易位t(8;11)而出现8号染色体短臂2区1带至末端(p21→pter)三体。该患儿的父亲及祖母携带相同的易位。
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