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	1.	[Analysis of evoked otoacoustic emissions in patients with high frequency cochlear hearing loss]. [electronic resource] by Ke, X M Producer: 19940629 In: Zhonghua er bi yan hou ke za zhi vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Nonsyndromic deafness and mitochondrial DNA mutation]. [electronic resource] by Liu, Y H Ke, X M Gu, Z P Producer: 20031006 In: Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	3.	Absorption mechanism of three curcumin constituents through in situ intestinal perfusion method. [electronic resource] by Wang, Y-H Ke, X-M Zhang, C-H Yang, R-P Producer: 20171006 In: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[Measuring and analyzing of otoacoustic emission tests of a family with genetic progressive sensorineural hearing loss]. [electronic resource] by Yu, H Ke, X M Yu, D L Li, Q Liu, Y H Ding, G Y Producer: 20030709 In: Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Genetic epidemiologic study of mitochondrial DNA 7445A-->G mutation among non-syndromic deafness in Chinese population]. [electronic resource] by Liu, Y H Ke, X M Qi, Y Xu, H B Gu, Z P Liu, X C Liu, J F Producer: 20030709 In: Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	6.	Audiological and genetic features of the mtDNA mutations. [electronic resource] by Liu, X Z Angeli, S Ouyang, X M Liu, W Ke, X M Liu, Y H Liu, S X Du, L L Deng, X W Yuan, H Yan, D Producer: 20081118 In: Acta oto-laryngologica vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome. [electronic resource] by Liu, X Z Hope, C Walsh, J Newton, V Ke, X M Liang, C Y Xu, L R Zhou, J M Trump, D Steel, K P Bundey, S Brown, S D Producer: 19981020 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)