WAGR syndrome is an acronym for the complex of symptoms seen in people who have the condition.
WAGR综合癥是具有这种状况的人身上观察到的综合癥的缩写。
In the current study, the NIH researchers conducted analyses of chromosome 11 in 33 patients with WAGR syndrome.
当前研究中,NIH的研究者分析了33名WAGR综合癥患者的11号染色体。
For this reason, the NIH researchers examined chromosome 11 from WAGR syndrome patients to learn if the gene for BDNF was affected, explained Dr. Yanovski.
由于这个原因,NIH的研究者研究WAGR综合癥患者的11号染色体,以获知是否也影响调节BDNF的基因,Yanovski博士解释到。
All people with WAGR syndrome lack two specific genes, called WT1 and PAX6, but each person can also be missing other nearby genes.
所有患有WAGR综合癥的患者都缺少两个称为WT1和PAX6的基因,但是每一个个体也可以丢失其它附近的基因。