机译:S162基因HAPLOUSUBUCKS导致可识别的表型,具有脑病,全龙酶发育不良和导电性听力损失
Genetikum Stuttgart Genet Counselling &
Diagnost Lautenschlagerstr 23 D-70173 Stuttgart Germany;
Klinikum Esslingen Dept Pediat Esslingen Germany;
Klinikum Esslingen Dept Pediat Esslingen Germany;
Genetikum Neu Ulm Genet Counselling &
Diagnost Neu Ulm Germany;
Genetikum Neu Ulm Genet Counselling &
Diagnost Neu Ulm Germany;
Genetikum Stuttgart Genet Counselling &
Diagnost Lautenschlagerstr 23 D-70173 Stuttgart Germany;
Genetikum Stuttgart Genet Counselling &
Diagnost Lautenschlagerstr 23 D-70173 Stuttgart Germany;
conductive hearing loss; frontonasal dysplasia; microdeletion 2p21; ptosis; SIX2 gene;
机译:S162基因HAPLOUSUBUCKS导致可识别的表型,具有脑病,全龙酶发育不良和导电性听力损失
机译:SIX2单倍剂量不足会导致人上睑下垂导致传导性听力损失
机译:六种臭氧水碎量导致人类皮毒性的导电性听力丧失
机译:扩张的心肌病和心律失常右心室发育不良:从基因到表型
机译:寻找传导性听力损失:行为测听测试,ASSR和SAL技术的比较。
机译:SIX2单倍剂量不足会导致人的上睑下垂传导性听力丧失
机译:六种臭氧水碎能导致人类的皮特病变丧失