528 related articles for article (PubMed ID: 9354819)
21. A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
Lopez GH; McGowan EC; McGrath KA; Abaca-Cleopas ME; Schoeman EM; Millard GM; O'Brien H; Liew YW; Flower RL; Hyland CA
Transfusion; 2016 Sep; 56(9):2322-30. PubMed ID: 27390888
[TBL] [Abstract][Full Text] [Related]
22. [Study on polymorphism of D gene exons among RhD-negative Chinese Han population].
Xu Q; Zhang S; Zhang J; Si G; Song Y; Wang M; Li J; Wang W; Nie X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):39-42. PubMed ID: 11172641
[TBL] [Abstract][Full Text] [Related]
23. A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.
Fichou Y; Le Maréchal C; Bryckaert L; Dupont I; Jamet D; Chen JM; Férec C
Transfusion; 2013 Nov; 53(11 Suppl 2):2974-82. PubMed ID: 23550903
[TBL] [Abstract][Full Text] [Related]
24. Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.
Silvy M; Simon S; Gouvitsos J; Di Cristofaro J; Ferrera V; Chiaroni J; Bailly P
Transfusion; 2011 Feb; 51(2):401-11. PubMed ID: 20723165
[TBL] [Abstract][Full Text] [Related]
25. RHCE-D-CE hybrid genes can cause false-negative DNA typing of the Rh e antigen.
Hundhausen T; Petershofen EK; Doescher A; Bauerfeind U; Müller TH; Schunter F
Vox Sang; 2002 Oct; 83(3):268-72. PubMed ID: 12366772
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.
Gassner C; Utz I; Schennach H; Ramoni A; Steiner H; Scholz S; Kreklau U; Körmöczi GF
Transfusion; 2013 Nov; 53(11 Suppl 2):2954-9. PubMed ID: 23550956
[TBL] [Abstract][Full Text] [Related]
28. Sensitive determination of the RhD genotype in mixed samples using fluorescence-based polymerase chain reaction.
Tonn T; Westrup D; Seidl C; Kirchmaier CM; Seifried E
Vox Sang; 1997; 72(3):177-81. PubMed ID: 9145489
[TBL] [Abstract][Full Text] [Related]
29. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes.
Rouillac C; Colin Y; Hughes-Jones NC; Beolet M; D'Ambrosio AM; Cartron JP; Le Van Kim C
Blood; 1995 May; 85(10):2937-44. PubMed ID: 7742554
[TBL] [Abstract][Full Text] [Related]
30. Effective molecular RHD typing strategy for blood donations.
Polin H; Danzer M; Hofer K; Gassner W; Gabriel C
Transfusion; 2007 Aug; 47(8):1350-5. PubMed ID: 17655577
[TBL] [Abstract][Full Text] [Related]
31. [Phenotype Types and Genetic Mutation Mechanism of Rhesus D Variant Individuals].
Luo H; Wen JZ; Zhang RQ; Ji YL; Mo CY; Wei L; Wang Z; Liao ZJ; Luo GP
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Dec; 25(6):1804-1809. PubMed ID: 29262920
[TBL] [Abstract][Full Text] [Related]
32. RHD 1227A is an important genetic marker for RhD(el) individuals.
Chen JC; Lin TM; Chen YL; Wang YH; Jin YT; Yue CT
Am J Clin Pathol; 2004 Aug; 122(2):193-8. PubMed ID: 15323135
[TBL] [Abstract][Full Text] [Related]
33. [Study on RHCE genotyping of Rh blood group in Uygur nationality of Xinjiang in China].
Bai XH; Lan JC; Gong XY; Cui L; Zhou HY
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1335-7. PubMed ID: 21129288
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Weak D type 1.1 exemplifies another complexity in weak D genotyping.
Doescher A; Flegel WA; Petershofen EK; Bauerfeind U; Wagner FF
Transfusion; 2005 Oct; 45(10):1568-73. PubMed ID: 16181206
[TBL] [Abstract][Full Text] [Related]
36. Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.
Ouchari M; Srivastava K; Romdhane H; Jemni Yacoub S; Flegel WA
Transfusion; 2018 Feb; 58(2):306-312. PubMed ID: 29193104
[TBL] [Abstract][Full Text] [Related]
37. Involvement of Ser103 of the Rh polypeptides in G epitope formation.
Faas BH; Beckers EA; Simsek S; Overbeeke MA; Pepper R; van Rhenen DJ; von dem Borne AE; van der Schoot CE
Transfusion; 1996 Jun; 36(6):506-11. PubMed ID: 8669081
[TBL] [Abstract][Full Text] [Related]
38. Clinically relevant RHD-CE genotypes in patients with sickle cell disease and in African Brazilian donors.
Gaspardi AC; Sippert EA; De Macedo MD; Pellegrino J; Costa FF; Castilho L
Blood Transfus; 2016 Sep; 14(5):449-54. PubMed ID: 27177398
[TBL] [Abstract][Full Text] [Related]
39. Accuracy of prenatal determination of RhD type status by polymerase chain reaction with amniotic cells.
Lighten AD; Overton TG; Sepulveda W; Warwick RM; Fisk NM; Bennett PR
Am J Obstet Gynecol; 1995 Oct; 173(4):1182-5. PubMed ID: 7485316
[TBL] [Abstract][Full Text] [Related]
40. RHD genotyping and its implication in transfusion practice.
Sassi A; Ouchari M; Houissa B; Romdhane H; Abdelkefi S; Chakroun T; Jemni Yacoub S
Transfus Apher Sci; 2014 Dec; 51(3):59-63. PubMed ID: 25457010
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
