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Items: 1 to 20 of 100

1.

The First Case of Para-Bombay Blood Type Encountered in a Korean Tertiary Hospital.

Kim MS, Kim JS, Park H, Chung Y, Kim H, Ko DH, Kim SH, Hwang SH, Oh HB.

J Korean Med Sci. 2019 Oct 14;34(39):e258. doi: 10.3346/jkms.2019.34.e258.

2.

Genomic analysis of para-Bombay individuals in south-eastern China: the possibility of linkage and disequilibrium between FUT1 and FUT2.

Zhang A, Chi Q, Ren B.

Blood Transfus. 2015 Jul;13(3):472-7. doi: 10.2450/2015.0185-14. Epub 2015 Jan 29.

3.

[Analysis on FUT1 and FUT2 gene of 10 para-Bombay individuals in China].

Guo ZH, Xiang D, Zhu ZY, Wang JL, Zhang JM, Liu X, Shen W, Chen HP.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Oct;21(5):417-21. Chinese.

PMID:
15476160
4.

[Molecular genetic analysis of FUT1 and FUT2 gene in para-Bombay Chinese: a novel FUT1 allele is identified].

Su Yq, Wei TL, Yu Q, Liang YL, Li DC.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):520-3. Chinese.

PMID:
17922418
5.

Molecular genetic analysis of para-Bombay phenotypes in Chinese: a novel non-functional FUT1 allele is identified.

Yip SP, Chee KY, Chan PY, Chow EY, Wong HF.

Vox Sang. 2002 Oct;83(3):258-62.

PMID:
12366770
6.

The summary of FUT1 and FUT2 genotyping analysis in Chinese para-Bombay individuals including additional nine probands from Guangzhou in China.

Luo G, Wei L, Wang Z, Luo H, Zhao Y, Zhang R, Mo C, Ji Y.

Transfusion. 2013 Dec;53(12):3224-9. doi: 10.1111/trf.12183. Epub 2013 Apr 8.

PMID:
23560544
7.

Four Non-functional FUT1 Alleles Were Identified in Seven Chinese Individuals with Para-Bombay Phenotypes.

Liang W, Cai F, Yang L, Zhang Z, Wang Z.

Iran J Public Health. 2018 Aug;47(8):1128-1136.

8.

A Very Rare Case with Particular H-deficient Phenotypes.

Song M, Zhao S, Jiang T, Lu H.

Indian J Hematol Blood Transfus. 2018 Oct;34(4):788-791. doi: 10.1007/s12288-018-0915-3. Epub 2018 Jan 11.

9.

Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual.

Wang L, Huang C, Wei Z, Tan J, Qin L, Tian L.

Transfusion. 2017 Jan;57(1):93-96. doi: 10.1111/trf.13879. Epub 2016 Dec 27.

PMID:
28026021
10.

Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.

Storry JR, Johannesson JS, Poole J, Strindberg J, Rodrigues MJ, Yahalom V, Levene C, Fujita C, Castilho L, Hustinx H, Olsson ML.

Transfusion. 2006 Dec;46(12):2149-55. Erratum in: Transfusion. 2007 Feb;47(2):360.

PMID:
17176328
11.

Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctional FUT1 allele.

Yan L, Zhu F, Xu X, Hong X, Lv Q.

Transfusion. 2005 May;45(5):725-30.

PMID:
15847661
12.

Identification of a Case with Heterozygous Mutations in the FUT1 Gene Leading to a Para-Bombay Phenotype.

Lin CL, Er TK.

Clin Lab. 2019 Dec 1;65(12). doi: 10.7754/Clin.Lab.2019.190602.

PMID:
31850709
13.

Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system.

Koda Y, Soejima M, Johnson PH, Smart E, Kimura H.

Biochem Biophys Res Commun. 1997 Sep 8;238(1):21-5.

PMID:
9299444
14.

A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.

Xu X, Tao S, Ying Y, Hong X, He Y, Zhu F, Lv H, Yan L.

Transfus Med. 2011 Dec;21(6):385-93. doi: 10.1111/j.1365-3148.2011.01111.x. Epub 2011 Oct 12.

PMID:
21988368
15.

[Mutational analysis for FUT1 gene in two cases with para-Bombay blood type].

Xu DY, Deng G, Huang DD, Zhao WJ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):694-8. doi: 10.3760/cma.j.issn.1003-9406.2011.06.022. Chinese.

PMID:
22161108
16.

Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.

Zanjani DS, Afzal Aghaee M, Badiei Z, Mehrasa R, Roodsarabi A, Khayyami ME, Shahabi M.

Vox Sang. 2016 Jul;111(1):88-92. doi: 10.1111/vox.12393. Epub 2016 Feb 29.

PMID:
26926997
17.

Heterozygous FUT1 Mutations Causing a Para-Bombay Phenotype.

Er TK, Yang TC, Liu YH.

Clin Lab. 2018 Oct 1;64(10):1787-1789. doi: 10.7754/Clin.Lab.2018.180428.

PMID:
30336518
18.

Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype.

Wang B, Koda Y, Soejima M, Kimura H.

Vox Sang. 1997;72(1):31-5. Erratum in: Vox Sang 1997;72(3):147.

PMID:
9031498
19.

Mutational Analysis of Bombay Phenotype in Iranian People: Identification of a Novel FUT1 Allele.

Roshan Mehr F, Manafi M, Sharifi Z, Shahabi M.

Indian J Hematol Blood Transfus. 2019 Apr;35(2):321-324. doi: 10.1007/s12288-018-1027-9. Epub 2018 Oct 8.

PMID:
30988570
20.

Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals.

Kelly RJ, Ernst LK, Larsen RD, Bryant JG, Robinson JS, Lowe JB.

Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5843-7.

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