fbxw4造句
造句与例句
手机版
- SHFM3 is unique in that it is caused by submicroscopic tandem chromosome duplications of FBXW4 / DACTYLIN . SHFM3 is considered'isolated'ectrodactyly and does not show a mutation of the tp63 gene.
- SHFM is a heterogeneous condition caused by abnormalities at one of multiple loci, including SHFM1 ( SHFM1 at 7q21-q22 ), SHFM2 ( Xq26 ), SHFM3 ( FBXW4 / DACTYLIN at 10q24 ), SHFM4 ( TP63 at 3q27 ), and SHFM5 ( DLX1 and DLX 2 at 2q31 ).
- It's difficult to see fbxw4 in a sentence. 用fbxw4造句挺难的