For example, achondroplasia, a common form of dwarfism, usually occurs as a result of a mutation at base pair 1138 in a gene called FGFR3 on the short arm of human chromosome 4.

 
  • 舉例來(lái)說(shuō),軟骨發(fā)育不全癥(achondroplasia,一種常見(jiàn)的侏儒癥)通常是人類(lèi)第四對染色體短臂上FGFR3這個(gè)基因的第1138個(gè)堿基對發(fā)生突變。
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