一例9号染色体短臂缺失综合征病例。
A case of 9p- syndrome.
作者信息
Kuroki Y, Yokota S, Nakai H, Yamamoto Y, Matsui I
出版信息
Hum Genet. 1977 Aug 31;38(1):107-11. doi: 10.1007/BF00295813.
PMID:903150
Abstract
An 8-month-old female child with the 9p- karyotype: 46,XX,del(9) (p22) is presented, being the first case from among Oriental people. She has many clinical features similar to those described in Caucasian cases.
摘要
本文报告了一名8个月大的女性儿童，其核型为9p-：46,XX,del(9)(p22)，这是东方人群中的首例。她有许多与高加索人病例中所描述的相似的临床特征。
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