Dergiler / Turkish Journal of Hematology / 2017 / Cilt: 34 - Sayı: 4

A Case of Para-Bombay Phenotype Caused by Homozygous Mutation of the FUT1 Gene

Sayfa
105–106
DOI
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Bu Makaleye Atıf Yap

ER, T., LİU, Y., YU, J. (2017). A Case of Para-Bombay Phenotype Caused by Homozygous Mutation of the FUT1 Gene. Turkish Journal of Hematology, Cilt: 34 - Sayı: 4, 105–106. https://ajindex.com/articles/413087

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Kaynakça (4)

  1. Cai XH, Jin X, Fan LF, Lu Q, Xiang D. Molecular genetic analysis for the paraBombay blood group revealing two novel alleles in the FUT1 gene. Blood Transfus 2011;9:466-468
  2. Chen DP, Tseng CP, Wang WT, Peng CT, Tsao KC, Wu TL, Lin KT, Sun CF. Two prevalent h allele in para-Bombay haplotypes among 250,000 Taiwanese. Ann Clin Lab Sci 2004;34:314-318
  3. Zhang A, Chi Q, Ren B. Genomic analysis of para-Bombay individuals in south-eastern China: the possibility of linkage and disequilibrium between FUT1 and FUT2. Blood Tranfus 2015;13:472-477
  4. Lin-Chu M, Broadberry RE. Blood transfusion in the para-Bombay phenotype. Br J Haematol 1990;75:568-572.