Webb T, Heath D
Department of Clinical Genetics, Maternity Hospital, Birmingham, U.K.
Cancer Genet Cytogenet. 1991 Oct 15;56(2):157-62. doi: 10.1016/0165-4608(91)90165-q.
Lymphocytes from a series of ten patients with von Hippel-Lindau syndrome have been cultured under conditions designed to demonstrate the presence of fragile sites. Compared to a series of controls the subjects with von Hippel-Lindau syndrome show a small but significant increase in the level of FRA3B.
对一系列10例冯·希佩尔-林道综合征患者的淋巴细胞在旨在证明脆性位点存在的条件下进行了培养。与一系列对照相比,冯·希佩尔-林道综合征患者的FRA3B水平有小幅但显著的升高。