1. A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome. Issue 4 (April 2017) Authors: Zheng, Bixia; Wang, Chunli; Jia, Zhanjun; Liu, Zhifeng; Li, Mei; Jin, Yu; Pan, Jian Journal: Journal of pediatric gastroenterology and nutrition Issue: Volume 64:Issue 4(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract. Issue 5 (24th January 2023) Authors: Kolvenbach, Caroline M.; Zheng, Bixia; Merz, Lea M.; Mertens, Nils D.; Mansour, Bshara; Wang, Chunyan; Seltzsam, Steve; Schneider, Sophia; Schierbaum, Luca; Pantel, Dalia; Chen, Jing; van der Ven, Amelie T.; Bello, Jibril O.; Shril, Shirlee; Hildebrandt, Friedhelm Journal: American journal of medical genetics Issue: Volume 191:Issue 5(2023) Page Start: 1355 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Antisense oligonucleotides rescue an intronic splicing variant in the ABCB11 gene that causes progressive familial intrahepatic cholestasis type 2. Issue 11 (November 2022) Authors: Zheng, Yucan; Zhou, Chunlei; Zheng, Bixia; Hu, Guorui; Wang, Chunli; Zhou, Wei; Lu, Yan; Zhang, Zhihua; Lin, Qian; Guo, Hongmei; Jin, Yu; Liu, Zhifeng; Tang, Weibing Journal: Digestive and liver disease Issue: Volume 54:Issue 11(2022) Page Start: 1541 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Association of AluYb8 insertion/deletion polymorphism in the MUTYH gene with mtDNA maintain in the type 2 diabetes mellitus patients. (5th July 2015) Authors: Guo, Wenwen; Zheng, Bixia; Guo, Dong; Cai, Zhenming; Wang, Yaping Journal: Molecular and cellular endocrinology Issue: Volume 409(2015) Page Start: 33 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Association of Base Excision Repair Gene Polymorphisms with ESRD Risk in a Chinese Population. (6th June 2012) Authors: Cai, Zhenming; Chen, Huimei; Tao, Jing; Guo, Wenwen; Liu, Xiufang; Zheng, Bixia; Sun, Wei; Wang, Yaping Other Names: Ksiazek Krzysztof Academic Editor. Journal: Oxidative medicine and cellular longevity Issue: Volume 2012(2012) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Functional Characterization of PHEX Gene Variants in Children With X‐Linked Hypophosphatemic Rickets Shows No Evidence of Genotype–Phenotype Correlation. (12th May 2020) Authors: Zheng, Bixia; Wang, Chunli; Chen, Qiuxia; Che, Ruochen; Sha, Yugen; Zhao, Fei; Ding, Guixia; Zhou, Wei; Jia, Zhanjun; Huang, Songming; Chen, Ying; Zhang, Aihua Journal: Journal of bone and mineral research Issue: Volume 35:Number 9(2020) Page Start: 1718 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system. Issue 5 (25th July 2019) Authors: Rao, Jia; Liu, Xiaorong; Mao, Jianhua; Tang, Xiaoshan; Shen, Qian; Li, Guomin; Sun, Li; Bi, Yunli; Wang, Xiang; Qian, Yanyan; Wu, Bingbing; Wang, Huijun; Zhou, Wenhao; Ma, Duan; Zheng, Bixia; Shen, Ying; Chen, Zhi; Luan, Jiangwei; Wang, Xiaowen; Wang, Mo Journal: Clinical genetics Issue: Volume 96:Issue 5(2019) Page Start: 402 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Highly compressible hydrogel sensors with synergistic long-lasting moisture, extreme temperature tolerance and strain-sensitivity properties. (30th September 2020) Authors: Liu, Zhenzhen; Liu, Jing; Zhang, Junmei; Zheng, Bixia; Ren, Xinle; Long, Yanjun; Fang, Liming; Ou, Rongxian; Liu, Tao; Wang, Qingwen Journal: Materials chemistry frontiers Issue: Volume 4:Number 11(2020) Page Start: 3319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. Issue 10 (19th June 2021) Authors: Lemire, Gabrielle; Zheng, Bixia; Ediae, Grace U.; Zou, Ruobing; Bhola, Priya T.; Chisholm, Caitlin; de Nanassy, Joseph; Lo, Bryan; Wang, Chunyan; Shril, Shirlee; El Desoky, Sherif; Shalaby, Mohammed; Kari, Jameela A.; Wang, Xueqi; Kernohan, Kristin D.; Boycott, Kym M.; Hildebrandt, Friedhelm; Saw... Journal: American journal of medical genetics Issue: Volume 185:Issue 10(2021) Page Start: 3005 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease. Issue 3 (13th January 2020) Authors: Ye, Qing; Shen, Qian; Rao, Jia; Zhang, Aihua; Zheng, Bixia; Liu, Xiaorong; Shen, Ying; Chen, Zhi; Wu, Yubing; Hou, Ling; Jian, Shan; Wei, Min; Ma, Mingsheng; Sun, Shuzhen; Li, Qian; Dang, Xiqiang; Wang, Ying; Xu, Hong; Mao, Jianhua Journal: Clinical genetics Issue: Volume 97:Issue 3(2020) Page Start: 407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗