因t(5;10)(p15;p11)导致的10号染色体短臂三体在一个大家系中分离。
Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship.
作者信息
Back E, Vogel W, Hertel C, Schuchmann L
出版信息
Hum Genet. 1978 Feb 23;41(1):11-7. doi: 10.1007/BF00278867.
PMID:631856
Abstract
A family is reported with a segregating t(5;10)(p15;p11) translocation resulting in a child carrying trisomy 10p. The clinical findings of the patient are compared with trisomy 10p and the Cri-du-Chat syndrome.
摘要
报道了一个家系，其中存在分离的t(5;10)(p15;p11)易位，导致一名儿童携带10号染色体短臂三体。将该患者的临床发现与10号染色体短臂三体及猫叫综合征进行了比较。
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