Neuroanatomical anomalies due to a defect in the FGF3 gene, associated with the Labyrinthine Aplasia, Microtia and Microdontia syndrome: insights from the placement of auditory brainstem implants in two siblings

FGF3基因缺陷导致的神经解剖异常，与迷路发育不全、小耳畸形和小牙畸形综合征相关：从两兄妹接受听觉脑干植入手术中获得的启示