A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).
作者信息
Bargman G J, Neu R L, Powers H O, Gardner L I
出版信息
J Med Genet. 1970 Mar;7(1):77-80. doi: 10.1136/jmg.7.1.77.
Abstract
摘要
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A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).一名患有多种先天性异常的女孩及其表型正常的父亲（46,XY,t(Cq+;Cq-)）存在46,XX,t(Cp+;Cq-)易位。
J Med Genet. 1970 Mar;7(1):77-80. doi: 10.1136/jmg.7.1.77.
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Ann Genet. 1968 Sep;11(3):171-5.
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