1. A novel B allele with c.736T>C, c.738C>A, and c.930A>G variations identified in a Chinese individual with Bw phenotype. Issue 4 (2nd March 2023) Authors: Zhang, Bing; Hong, Xiaozhen; Xu, Xianguo; Zhu, Faming Journal: Transfusion Issue: Volume 63:Issue 4(2023) Page Start: E25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel mutation in A4GALT was identified in a Chinese individual with p phenotype. Issue 1 (9th September 2016) Authors: Li, Xiaofei; Diao, Xueqin; Xia, Xiaoye; Hong, Xiaozhen; Zhu, Faming Journal: Transfusion Issue: Volume 57:Issue 1(2017) Page Start: 215 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. ABO antigen levels on platelets of normal and variant ABO blood group individuals. (3rd October 2019) Authors: Xu, Xianguo; Xu, Fang; Ying, Yanling; Hong, Xiaozhen; Liu, Ying; Chen, Shu; He, Ji; Zhu, Faming; Hu, Wei Journal: Platelets Issue: Volume 30:Number 7(2019) Page Start: 854 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. C.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype. Issue 10 (11th September 2018) Authors: Li, Xiaofei; Li, Aijun; Xia, Xiaoye; Wang, Deqing; Zhu, Faming Journal: Transfusion Issue: Volume 58:Issue 10(2018) Page Start: 2467 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. C.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype. Issue 10 (5th September 2019) Authors: Chen, Shu; Hong, Xiaozhen; Xu, Xianguo; Ma, Kairong; He, Ji; Zhu, Faming Journal: Transfusion Issue: Volume 59:Issue 10(2019) Page Start: E4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. C.49T>C mutation on the α‐(1, 2)‐fucosyltransferase gene responsible for an individual with para‐Bombay phenotype. Issue 4 (13th February 2018) Authors: Hong, Xiaozhen; Chen, Shu; Ma, Kairong; He, Ji; Zhu, Faming Journal: Transfusion Issue: Volume 58:Issue 4(2018) Page Start: 1076 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. C.518T > C missense mutation in the B glycosyltransferase gene responsible for a weak B variant. Issue 1 (6th November 2017) Authors: Ying, Yanling; Hong, Xiaozhen; Chen, Shu; He, Ji; Zhu, Faming Journal: Transfusion Issue: Volume 58:Issue 1(2018) Page Start: 269 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. C.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype. Issue 10 (25th June 2019) Authors: Hong, Xiaozhen; Chen, Shu; Ma, Kairong; He, Ji; Zhu, Faming Journal: Transfusion Issue: Volume 59:Issue 10(2019) Page Start: E11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Characterization of the novel HLA allele: HLA‐B*15:437 in a Chinese bone marrow donor. (8th June 2020) Authors: Wang, Fang; You, Xuan; Zhang, Wei; He, Ji; Zhu, Faming Journal: HLA Issue: Volume 96:Number 4(2020) Page Start: 511 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Characterization of the novel HLA‐A*11:280 allele by next‐generation sequencing in a Chinese cord blood donor. (20th January 2020) Authors: Dong, Lina; Wang, Fang; You, Xuan; He, Ji; Zhu, Faming Journal: HLA Issue: Volume 95:Number 5(2020) Page Start: 482 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗