Feng Z - Search Results

1

A novel FUT1 variant allele was identified in a Chinese Para-Bombay individual.

Han B, Zhu J, Zhu Y, Feng Z, Zhang S. Han B, et al. Among authors: feng z. Transfusion. 2022 Jan;62(1):E1-E2. doi: 10.1111/trf.16712. Epub 2021 Oct 24. Transfusion. 2022. PMID: 34693534 No abstract available.

2

[Sequence Analysis of A Novel HLA-B*13:68 Allele].

Han B, Han L, Feng ZH, Chi XY, Jiao SX. Han B, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2015 Aug;23(4):1144-6. doi: 10.7534/j.issn.1009-2137.2015.04.045. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2015. PMID: 26314461 Chinese.

3

[Study on Molecular Biology of Rare Two A307 Phenotypes].

Han B, Feng ZH, Guo QM, Wang MM. Han B, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Jun;24(3):918-20. doi: 10.7534/j.issn.1009-2137.2016.03.051. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 27342533 Chinese.

4

[Serological and molecular study of three cases with a rare Bx02 blood group].

Han B, Liu P, Liu X, Feng Z. Han B, et al. Among authors: feng z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):65-67. doi: 10.3760/cma.j.issn.1003-9406.2017.01.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28186597 Chinese.

5

[Polymorphism of RHD gene among RhD negative and D variant blood donors from Qingdao region].

Hu B, Feng Z, Zhu Y. Hu B, et al. Among authors: feng z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):897-900. doi: 10.3760/cma.j.issn.1003-9406.2017.06.026. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188626 Chinese.

6

A novel A allele with c.689G>T mutation identified in a Chinese individual.

Ma W, Feng Z, Hu B, Han B, Jiao S. Ma W, et al. Among authors: feng z. Transfusion. 2018 Sep;58(9):2250-2251. doi: 10.1111/trf.14803. Epub 2018 Aug 24. Transfusion. 2018. PMID: 30144089 No abstract available.

7

A new RHD variant allele in Exon 2 identified in a Chinese individual.

Zhu Y, Feng Z, Lyu H, Jiao S, Hu B. Zhu Y, et al. Among authors: feng z. Transfusion. 2019 Feb;59(2):791-792. doi: 10.1111/trf.15073. Epub 2018 Dec 11. Transfusion. 2019. PMID: 30548271 No abstract available.

8

A new missense mutation c.692C>A caused a weak Ael phenotype in a Chinese individual.

Yu S, Feng Z, Ma W, Yan P. Yu S, et al. Among authors: feng z. Transfusion. 2019 Oct;59(10):E6-E7. doi: 10.1111/trf.15503. Transfusion. 2019. PMID: 31595994 No abstract available.

9

A novel A allele with c.499G>A mutation identified in a Chinese individual.

Han B, Liu L, Feng Z, Bu X. Han B, et al. Among authors: feng z. Transfusion. 2020 Jun;60(6):E15-E16. doi: 10.1111/trf.15804. Epub 2020 Apr 24. Transfusion. 2020. PMID: 32333385 No abstract available.

10

A novel A allele with c.287G > T mutation identified in a Chinese family.

Ma W, Zhang S, Jiao S, Feng Z. Ma W, et al. Among authors: feng z. Transfusion. 2020 Jul;60(7):E19-E20. doi: 10.1111/trf.15862. Epub 2020 Jun 1. Transfusion. 2020. PMID: 32483846 No abstract available.

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