因父源性t(8;20)易位导致的20q部分三体。病例报告及文献复习。
Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literature.
作者信息
Pierquin G, Herens C, Dodinval P, Frederic J, Weber I, Senterre J, Fryns J P
机构信息
Department of Human Genetics, University of Liege, Belgium.
出版信息
Clin Genet. 1988 May;33(5):386-9. doi: 10.1111/j.1399-0004.1988.tb03466.x.
Abstract
In this report we present a malformed female newborn with partial trisomy 20q who was the unbalanced product of a paternal 8p/20q translocation (46,XY,t(8;20) (p23.1;q11].
摘要
在本报告中，我们呈现了一名患有20q部分三体的畸形女新生儿，她是父源性8p/20q易位（46,XY,t(8;20)(p23.1;q11])的不平衡产物。
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