These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
143 related articles for article (PubMed ID: 9633555)
1. RHD genotyping in weak D phenotypes by multiple polymerase chain reactions. Legler TJ; Maas JH; Blaschke V; Malekan M; Ohto H; Lynen R; Bustami N; Schwartz DW; Mayr WR; Köhler M; Panzer S Transfusion; 1998 May; 38(5):434-40. PubMed ID: 9633555 [TBL] [Abstract][Full Text] [Related]
2. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features. Wagner FF; Gassner C; Muller TH; Schonitzer D; Schunter F; Flegel WA Blood; 1998 Mar; 91(6):2157-68. PubMed ID: 9490704 [TBL] [Abstract][Full Text] [Related]
3. An easy RHD genotyping strategy for D- East Asian persons applied to Korean blood donors. Luettringhaus TA; Cho D; Ryang DW; Flegel WA Transfusion; 2006 Dec; 46(12):2128-37. PubMed ID: 17176325 [TBL] [Abstract][Full Text] [Related]
4. Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Avent ND; Martin PG; Armstrong-Fisher SS; Liu W; Finning KM; Maddocks D; Urbaniak SJ Blood; 1997 Apr; 89(7):2568-77. PubMed ID: 9116304 [TBL] [Abstract][Full Text] [Related]
6. [Molecular background of weak D type 15 as the predominant weak D type found in Chinese population]. Sun GD; Duan XM; Zhang YP; Yin ZZ; Niu XL; Li YF; Zhao YL; Niu HJ Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2006 Oct; 14(5):1024-8. PubMed ID: 17096912 [TBL] [Abstract][Full Text] [Related]
7. Random survey for RHD alleles among D+ European persons. Chen Q; Flegel WA Transfusion; 2005 Jul; 45(7):1183-91. PubMed ID: 15987365 [TBL] [Abstract][Full Text] [Related]
8. [Rh-D genotyping for exon 2, 5 and 7 of German and Japanese blood donors with sequence specific polymerase chain reaction]. Maas JH; Legler TJ; Lynen R; Blaschke V; Ohto H; Köhler M Beitr Infusionsther Transfusionsmed; 1997; 34():203-9. PubMed ID: 9417341 [TBL] [Abstract][Full Text] [Related]
9. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons. Maaskant-van Wijk PA; Faas BH; de Ruijter JA; Overbeeke MA; von dem Borne AE; van Rhenen DJ; van der Schoot CE Transfusion; 1998; 38(11-12):1015-21. PubMed ID: 9838930 [TBL] [Abstract][Full Text] [Related]
10. Partial D phenotypes and genotypes in the Chinese population. Ye L; Wang P; Gao H; Zhang J; Wang C; Li Q; Han S; Guo Z; Yang Y; Zhu Z Transfusion; 2012 Feb; 52(2):241-6. PubMed ID: 21790636 [TBL] [Abstract][Full Text] [Related]
11. An effective diagnostic strategy for accurate detection of RhD variants including Asian DEL type in apparently RhD-negative blood donors in Korea. Seo MH; Won EJ; Hong YJ; Chun S; Kwon JR; Choi YS; Kim JN; Lee SA; Lim AH; Kim SH; Park KU; Cho D Vox Sang; 2016 Nov; 111(4):425-430. PubMed ID: 27864976 [TBL] [Abstract][Full Text] [Related]
12. [Molecular basis of Rh DEL phenotype in Zhejiang Han population]. Chen AX; Wu JJ; Xu FJ; Zhang LY; Ni YH; Fu QH Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2006 Oct; 14(5):1029-32. PubMed ID: 17096913 [TBL] [Abstract][Full Text] [Related]
13. Molecular and Family Analyses of a Novel RHD1058G>C Allele in a Chinese RhD Population. Wang Y; Zhou R; Hong WX; Wang X; Zhang Z; Gu J; Wang X; Wu CL; Shao C Clin Lab; 2024 Mar; 70(3):. PubMed ID: 38469779 [TBL] [Abstract][Full Text] [Related]
14. Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese. Shao CP; Maas JH; Su YQ; Köhler M; Legler TJ Vox Sang; 2002 Aug; 83(2):156-61. PubMed ID: 12201845 [TBL] [Abstract][Full Text] [Related]
15. [Exon polymorphism of human RHD gene]. Zhou HY; Lan JC; Wang XZ; Wang Y; Fan H; Meng QB; Gong HW Di Yi Jun Yi Da Xue Xue Bao; 2004 May; 24(5):513-6. PubMed ID: 15151820 [TBL] [Abstract][Full Text] [Related]
16. RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes. Cruz BR; Chiba AK; Moritz E; Bordin JO Transfus Med; 2012 Apr; 22(2):84-9. PubMed ID: 22211984 [TBL] [Abstract][Full Text] [Related]
17. D(Va) category phenotype and genotype in Japanese families. Legler TJ; Wiemann V; Ohto H; Matuda I; Obara T; Uchikawa M; Köhler M Vox Sang; 2000; 78(3):194-7. PubMed ID: 10838521 [TBL] [Abstract][Full Text] [Related]
18. D variants in the population of D-negative blood donors in the north-eastern region of Croatia. Safic Stanic H; Dogic V; Herceg I; Jagnjic S; Bingulac-Popovic J; Babic I; Corusic A; Jukic I Transfus Med; 2021 Feb; 31(1):43-47. PubMed ID: 33034130 [TBL] [Abstract][Full Text] [Related]
19. Serological and molecular characterisation of the most prevalent weak D variants in Croatian population. Stanic HS; Galic ZK; Dogic V; Bingulac-Popovic J; Jukic I Transfus Med; 2023 Apr; 33(2):132-136. PubMed ID: 36453092 [TBL] [Abstract][Full Text] [Related]
20. Molecular biology of partial D phenotypes. Avent ND; Finning KM; Liu W; Scott ML Transfus Clin Biol; 1996; 3(6):511-6. PubMed ID: 9018818 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]