A novel RHD allele caused by RHD c.710_713dup associated with a negative phenotype in a Chinese Han blood donor von Wu, Fan, Zhuang, Nai‐Bao, Liang, Shuang, Peng, Long, Liang, Yan‐lian, Su, Yu‐qing

Volltext

Identification of a novel A allele with a c.36‐39delA on the ABOA1.02 allele von Liang, Shuang, Liang, Yan‐Lian, Su, Yu‐Qing, Wu, Fan, Peng, Long, Xu, Yun‐ping

Volltext

Naturally occurring anti‐PP1PK in a Chinese individual with p phenotype: A case based on compound heterozygosity including one novel allele von Liang, Shuang, Wu, Fan, Deng, Zhi‐Hui, Liang, Yan‐Lian, Peng, Long, Su, Yu‐Qing

Volltext

A novel GYPA01 allele with a c.125C > G (p.Thr42Ser) mutation identified in a Chinese individual von Liang, Yan‐Lian, Liang, Shuang, Tang, Xiong‐Chi, Su, Yu‐Qing, Wu, Fan, Peng, Long, Xu, Yun‐Ping

Volltext

A new RHD variant allele caused by an RHD c.1228‐1G>C mutation in a Chinese family von Wu, Fan, Liang, Shuang, Zhuang, Nai‐Bao, Su, Yu‐Qing, Liang, Yan‐Lian, Peng, Long, Xu, Yun‐Ping, Shao, Chao‐Peng

Volltext

Identification of a novel B allele with a c.917 T > C mutation on the ABOB.01 allele von Liang, Shuang, Su, Yu‐Qing, Liang, Yan‐Lian, Wu, Fan, Peng, Long, Xu, Yun‐ping

Volltext

Maternal Cold-Reacting Immunoglobulin G Anti-M of MNS Blood Group System Causing Hemolytic Disease of the Fetus von Liang, Yan-Lian, Shi, Yu, Su, Yu-Qing, Wu, Fan, Liang, Yanwen, Fan, Xiuchu, Lin, Jiansuo, Liu, Yi, Long, Peng, Ren, Jianwei, Liang, Shuang

Volltext

Characterization of a novel B(A) allele with BBBA type at the ABO blood group von Deng, Zhi-Hui, Yu, Qiong, Liang, Yan-Lian, Wang, Da-Ming, Su, Yu-Qing, Wu, Guo-Guang

Volltext

Haemolytic disease of fetus and newborn caused by ABO antibodies in a cisAB offspring von Deng, Zhi-Hui, Seltsam, Axel, Ye, You-Wan, Yu, Qiong, Li, Qian, Su, Yu-Qing, Liang, Yan-Lian, Zang, Hao

Volltext

Genotyping of samples lacking expected antibodies in ABO blood group von Deng, Zhi-Hui, Zeng, Jian-Qiang, Yu, Qiong, Su, Yu-Qing, Liang, Yan-Lian, Lu, Liang, Zhu, Wei-Gang, Yang, Bao-Cheng

Volltext

Naturally occurring anti‐PP1P K in a Chinese individual with p phenotype: A case based on compound heterozygosity including one novel allele von Liang, Shuang, Wu, Fan, Deng, Zhi‐Hui, Liang, Yan‐Lian, Peng, Long, Su, Yu‐Qing

Volltext

Identification of a novel A allele with a c. 36‐39delA on the ABO A1 .02 allele von Liang, Shuang, Liang, Yan‐Lian, Su, Yu‐Qing, Wu, Fan, Peng, Long, Xu, Yun‐ping

Volltext

Identification of a novel B allele with a c.917T >C mutation on the ABOB.01 allele von Liang, Shuang, Yu‐Qing Su, Yan‐Lian Liang, Wu, Fan, Long, Peng, Yun‐ping Xu

Volltext

A Chinese individual with DEL phenotype caused by a novel RHD allele von Wu, Fan, Luo, Ya-dan, Liang, Shuang, Sun, Li-yan, Liu, Tong, Liang, Yan-lian, Su, Yu-qing

Volltext

A new RHD variant allele caused by an RHD c. 1228‐1G >C mutation in a Chinese family von Wu, Fan, Liang, Shuang, Zhuang, Nai‐Bao, Su, Yu‐Qing, Liang, Yan‐Lian, Peng, Long, Xu, Yun‐Ping, Shao, Chao‐Peng

Volltext

Molecular polymorphism of O alleles in the Chinese Han population von Yang, Bao-Cheng, Zeng, Jian-Qiang, Yu, Qiong, Liang, Yan-Lian, Su, Yu-Qing, Deng, Zhi-Hui

Volltext

DNA sequence analysis and Jk blood group genotype-phenotype assessment von Liang, Shuang, Su, Yu-Qing, Liang, Yan-Lian, Wu, Fan, Zhang, Hao, Shi, Jia-Hai, Hong, Wen-Xu, Xu, Yun-Ping

Volltext

Polymorphic analysis of the Lutheran blood group system in Chinese von Zeng, Jian Qiang, Deng, Zhi Hui, Yang, Bao Cheng, Liang, Yan Lian, Su, Yu Qing, Li, Da Cheng, Yu, Qiong

Volltext

Noninvasive genotyping of 9 Y-chromosome specific STR loci using circulatory fetal DNA in maternal plasma by multiplex PCR von Deng, ZhiHui, Wu, GuoGuang, Li, Qian, Zhang, Xuan, Liang, YanLian, Li, DaCheng, Gao, SuQing, Lan, YuXiao

Volltext

Haemolytic disease of fetus and newborn caused by ABO antibodies in a cis AB offspring von Deng, Zhi-Hui, Seltsam, Axel, Ye, You-Wan, Yu, Qiong, Li, Qian, Su, Yu-Qing, Liang, Yan-Lian, Zang, Hao

Volltext