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	1.	Novel mutation of OCRL1 in Lowe syndrome. [electronic resource] by Liu, Ting Yue, Zhihui Wang, Haiyan Tong, Huajuan Sun, Liangzhong Producer: 20161110 In: Indian journal of pediatrics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Clinical features and mutation of NPHP5 in two Chinese siblings with Senior-Løken syndrome. [electronic resource] by Tong, Huajuan Yue, Zhihui Sun, Liangzhong Chen, Huiqin Wang, Weiguang Wang, Haiyan Producer: 20141126 In: Nephrology (Carlton, Vic.) vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients. [electronic resource] by Sun, Liangzhong Tong, Huajuan Wang, Haiyan Yue, Zhihui Liu, Ting Lin, Hongrong Li, Jun Wang, Changxi Producer: 20161026 In: Nephrology (Carlton, Vic.) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis. [electronic resource] by Yue, Zhihui Lin, Hongrong Li, Min Wang, Haiyan Liu, Ting Hu, Miaoyue Chen, Huamu Tong, Huajuan Sun, Liangzhong Producer: 20210125 In: Clinica chimica acta; international journal of clinical chemistry vol. 506 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)