伴有相互易位t(1;17)(q25;q21)的先天性甲状腺功能亢进症。
Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21).
作者信息
Gregori-Romero M, López-Ginés C, Gil R, Pellín A
机构信息
Department of Pathology, Faculty of Medicine, University of Valencia, Spain.
出版信息
Hum Genet. 1989 Sep;83(2):203. doi: 10.1007/BF00286721.
PMID:2777262
Abstract
The authors report a case of 1;17 translocation and request contact with colleagues who have observed similar cases.
摘要
作者报告了一例1;17易位病例，并请求与观察到类似病例的同事取得联系。
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