1. A novel B allele with c.28 + 5885C>T substitution in the erythroid cell–specific regulatory element identified in an individual with phenotype B3. Issue 5 (20th April 2017) Authors: Tao, Cuihua; Xiao, Jianyu; Hu, Yuanping; Huang, Chengyin; Sun, Jun; Li, Min; Chen, Qing Journal: Transfusion Issue: Volume 57:Issue 5(2017) Page Start: 1318 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel B allele with c.502C>G mutation identified in a Chinese individual. Issue 6 (21st November 2014) Authors: Chen, Qing; Xiao, Jianyu; Lu, Le; Du, Leilei; Huang, Chengyin; Li, Min; Li, Ping; Yao, Genhong Journal: Transfusion Issue: Volume 55:Issue 6(2015)Part 2 Page Start: 1582 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A null allele caused by a four‐base‐pair duplication within the RHCE gene encoding a D– – phenotype. Issue 3 (3rd December 2020) Authors: Chen, Qing; Xiao, Jianyu; Zhang, Min; Huang, Chengyin; Li, Min; Flegel, Willy A.; Zhou, Xiaoyu Journal: Transfusion Issue: Volume 61:Issue 3(2021) Page Start: E23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype. Issue 9 (29th July 2021) Authors: Feng, Chenchen; Li, Hui; Liu, Taixiang; Xiao, Jianyu; Huang, Chengyin; Flegel, Willy A.; Chen, Qing Journal: Transfusion Issue: Volume 61:Issue 9(2021) Page Start: E59 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genotype frequency of human neutrophil antigen‐3 polymorphisms in the Yi, Han, and Tibetan populations of China. Issue 3 (23rd November 2015) Authors: Chen, Qing; Srivastava, Kshitij; Liu, Zhong; Xiao, Jianyu; Huang, Chengyin; Sun, Jun; Li, Min; Flegel, Willy Albert Journal: Transfusion Issue: Volume 56:Issue 3(2016:Mar.) Page Start: 737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel A4GALT gene variation with rare p phenotype in a compound heterozygous Chinese individual. Issue 1 (28th October 2020) Authors: Chen, Qing; Xiao, Jianyu; Duan, Zhimin; Shi, Lili; Huang, Chengyin; Li, Min Journal: Transfusion Issue: Volume 61:Issue 1(2021) Page Start: E5 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The prevalence of human T‐cell leukemia virus in blood donors in China. Issue 7 (15th April 2019) Authors: Li, Ling; Ou, Shanhai; Huang, Chengyin; Zhou, Xueyong; Ge, Hongwei; Li, Jianping; Zeng, Jinfeng; Zhou, Alyssa; He, Liu; Xu, Quming; Wu, Jie; Li, Longhuo; Wang, Chenghui; Zang, Liang; Huang, Liqin; Niu, Libin; Han, Hui; Zhang, Gang; Wan, Jianhua; Wang, Fang Journal: Transfusion Issue: Volume 59:Issue 7(2019) Page Start: 2361 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. What is the meaning of a nonresolved viral nucleic acid test–reactive minipool?. Issue 2 (15th August 2014) Authors: Wang, Lunan; Chang, Le; Xie, Yunzheng; Huang, Chengyin; Xu, Lei; Qian, Rong; Zhu, Haifeng; He, Yaqin; Li, Jing; Huang, Hongliang; Li, Wen; Zhang, Kuo; Zhang, Rui; Xie, Jiehong; Sun, Yu; Li, Jinming Journal: Transfusion Issue: Volume 55:Issue 2(2015) Page Start: 395 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗