Article
Molecular analysis of inactive and active RHD alleles in native Congolese cohorts. Touinssi M, Chapel-Fernandes S, Granier T, Bokilo A, Bailly P, Chiaroni J. Transfusion, 2009. [Citation]
Annotations by Allele
- RHD deletion (RHD*01N.01): otherHaplotype
- RHD deletion (RHD*01N.01): Prevalence
- RHD deletion (RHD*01N.01): Prevalence
- RHD deletion (RHD*01N.01): RH1
- RHD or DIIIa-CEVS(4-7)-D - partly characterized or subtypes not separated: RH1 (adsorption-elution was not performed)
- RHD or DIIIa-CEVS(4-7)-D - partly characterized or subtypes not separated: otherHaplotype
- RHD or DIIIa-CEVS(4-7)-D - partly characterized or subtypes not separated: Prevalence
- RHD or DIIIa-CEVS(4-7)-D - partly characterized or subtypes not separated: Prevalence
- RHD*1136T (DAU0): Prevalence
- RHD*1136T (DAU0): Prevalence
- RHD*1136T (DAU0): Prevalence
- RHD*1136T (DAU0): Prevalence
- RHD*186T,410T,455C (DIII type 4): Prevalence
- RHD*186T,410T,455C,1048C (DIVa): Prevalence
- RHD*186T,410T,455C,602G,667G,819A (DIIIa): Prevalence
- RHD*602G,667G (weak D type 4.0.1, DAR3): otherHaplotype
- RHD*602G,667G (weak D type 4.0.1, DAR3): otherHaplotype
- RHD*602G,667G (weak D type 4.0.1, DAR3): Prevalence
- RHD*602G,667G (weak D type 4.0.1, DAR3): RH1 (by direct agglutination)
- RHD*602G,667G,744T,1025C (weak D type 4.2.3, DAR1.03): RH1 (by direct agglutination)
- RHD*602G,667G,744T,1025C (weak D type 4.2.3, DAR1.03): Prevalence
- RHD*602G,667G,744T,1025C (weak D type 4.2.3, DAR1.03): otherHaplotype
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): Prevalence
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): RH1 (by direct agglutination)
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): otherHaplotype
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): Prevalence
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
- RHD*602G,667G,957A,1025C (weak D type 4.2.1, DAR1.01): Prevalence
- RHD*667G,697C (DV type 1, Kou): Prevalence
- RHD*667G,697C,1136T (DAU5): Prevalence
- RHD*667G,697C,1136T (DAU5): Prevalence
- RHD*835A,1136T (DAU3): Prevalence
- RHD*835A,1136T (DAU3): Prevalence
- RHD*835A,1136T (DAU3): Prevalence
- RHD*835A,998A,1136T (DAU7): Prevalence
- RHD*835A,998A,1136T (DAU7): RH1
- RHD*998A,1136T (DAU6): Prevalence
- RHD*Dpsi (RHD*08N.01): Prevalence
- RHD*Dpsi (RHD*08N.01): Prevalence
- RHD*Dpsi (RHD*08N.01): RH1
- RHD*Dpsi (RHD*08N.01): otherHaplotype
- RHD*Dpsi (RHD*08N.01): otherHaplotype
- RHD*Dpsi (RHD*08N.01): Prevalence
- RHD*Dpsi (RHD*08N.01): Prevalence
- standard RHD (RHD*01): Prevalence
- standard RHD (RHD*01): Prevalence
- standard RHD (RHD*01): Prevalence
- standard RHD (RHD*01): Prevalence
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: RH1 (by direct agglutination)
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: otherHaplotype
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: Prevalence
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: Prevalence