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	1.	A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China. [electronic resource] by Zhu, Junzhen Cao, Qinying Zhang, Ning Ge, Jun Sun, Donglan Feng, Qingqi Producer: 20150912 In: Intractable & rare diseases research vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Prenatal diagnosis and genetic counseling in two pedigrees affected with infantile polycystic kidney disease due to PKHD1 gene mutations]. [electronic resource] by Cao, Qinying Zhang, Weixia Ge, Jun Sun, Donglan Feng, Qingqi Li, Caixia Meng, Yucui Zhu, Junzhen Producer: 20190924 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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