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2. ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.

3. A null allele caused by a four‐base‐pair duplication within the RHCE gene encoding a D– – phenotype.

4. Genotype frequency of human neutrophil antigen-3 polymorphisms in the Yi, Han, and Tibetan populations of China.

5. Incidence and clinical implication of tumor cavitation in patients with advanced non-small cell lung cancer induced by Endostar, an angiogenesis inhibitor.

6. Novel A4GALT gene variation with rare p phenotype in a compound heterozygous Chinese individual.

7. Circulating endothelial cells and tumor blood volume as predictors in lung cancer.

8. A novel B allele with c.28 + 5885C>T substitution in the erythroid cell-specific regulatory element identified in an individual with phenotype B3.

9. A novel B allele with c.28 + 5885C>T substitution in the erythroid cell-specific regulatory element identified in an individual with phenotype B3.

10. A novel B allele with c.502 C> G mutation identified in a Chinese individual.

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