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Items: 1 to 20 of 135

1.

Detection of a novel large deletion causing α-thalassemia in South China.

Jia X, Huang R, Lei Z, Yao L, Wang L, Li Y, Meng D, Zhou Y, Liu J, Zhang X.

Exp Mol Pathol. 2013 Aug;95(1):68-73. doi: 10.1016/j.yexmp.2013.05.007.

PMID:
23726795
2.

[Rapid detection of three common deletional alpha thalassemias in Chinese by single-tube multiplex PCR].

Zhou Y, Zhang Y, Li L, Li W, Mo Q, Zheng Q, Xu X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):180-4. Chinese.

PMID:
15793780
3.

Detection of alpha-thalassemia in China by using multiplex ligation-dependent probe amplification.

Liu JZ, Han H, Schouten JP, Wang LR, Fan XP, Duarte HB, Zhu CJ, Cai R, Xiao B, Wang QT.

Hemoglobin. 2008;32(6):561-71. doi: 10.1080/03630260802508111.

PMID:
19065334
4.

A multiplex qPCR gene dosage assay for rapid genotyping and large-scale population screening for deletional α-thalassemia.

Zhou W, Wang G, Zhao X, Xiong F, Zhou S, Peng J, Cheng Y, Xu S, Xu X.

J Mol Diagn. 2013 Sep;15(5):642-51. doi: 10.1016/j.jmoldx.2013.05.007. Erratum in: J Mol Diagn. 2013 Nov;15(6):840.

PMID:
23810501
5.
6.

Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletions.

Fallah MS, Mahdian R, Aleyasin SA, Jamali S, Hayat-Nosaeid M, Karimipour M, Raeisi M, Zeinali S.

Blood Cells Mol Dis. 2010 Jun 15;45(1):58-64. doi: 10.1016/j.bcmd.2010.03.001.

PMID:
20363165
7.

Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli Arabs.

Gilad O, Dgany O, Noy-Lotan S, Krasnov T, Elitzur S, Pissard S, Kventsel I, Yacobovich J, Tamary H.

Hemoglobin. 2014;38(5):319-24. doi: 10.3109/03630269.2014.954668.

PMID:
25222045
8.

Frequencies of HKαα and anti-HKαα Alleles in Chinese Carriers of Silent Deletional α-Thalassemia.

Wu MY, Li J, Li SC, Li Y, Li DZ.

Hemoglobin. 2015;39(6):407-11. doi: 10.3109/03630269.2015.1071268.

PMID:
26287669
9.

Molecular characterization of a novel 27.6-kb deletion causing α(+) thalassemia in a Chinese family.

Wei XF, Shang X, He DQ, Huang JW, Zhang XH, Xu XM.

Ann Hematol. 2011 Jan;90(1):17-22. doi: 10.1007/s00277-010-1030-1.

PMID:
20645100
10.

A rapid detection for α-thalassemia by PCR combined with dissociation curve analysis.

Jia X, Liu J, Wang L, Yao L, Tang N, Cai R, Xiao B.

Exp Mol Pathol. 2011 Oct;91(2):626-30. doi: 10.1016/j.yexmp.2011.06.013.

PMID:
21806986
11.
12.

Detection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting analysis.

Pornprasert S, Wiengkum T, Srithep S, Chainoi I, Singboottra P, Wongwiwatthananukit S.

Korean J Lab Med. 2011 Jul;31(3):138-42. doi: 10.3343/kjlm.2011.31.3.138.

13.

Development and evaluation of a reverse dot blot assay for the simultaneous detection of common alpha and beta thalassemia in Chinese.

Lin M, Zhu JJ, Wang Q, Xie LX, Lu M, Wang JL, Wang CF, Zhong TY, Zheng L, Pan MC, Wu JR, Wen YF, Liu GR, Zhan XF, Lin F, Yang LY.

Blood Cells Mol Dis. 2012 Feb 15;48(2):86-90. doi: 10.1016/j.bcmd.2011.12.001.

PMID:
22197394
15.

Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.

Brieghel C, Birgens H, Frederiksen H, Hertz JM, Steenhof M, Petersen J.

Hemoglobin. 2015;39(5):346-9. doi: 10.3109/03630269.2015.1054512.

PMID:
26114741
16.

Heterogeneity in alpha-thalassemia interactions in Malays, Chinese and Indians in Malaysia.

Wee YC, Tan KL, Chow TW, Yap SF, Tan JA.

J Obstet Gynaecol Res. 2005 Dec;31(6):540-6.

PMID:
16343256
17.

Clinical and molecular characterization of a rare 2.4 kb deletion causing α(+) thalassemia in a Chinese family.

Lin M, Wu JR, Huang Y, Lin F, Zhan XF, Lin CP, Tong X, Luo ZY, Yang HT, Yang LY, Wang Q, Zheng L, Zhong TY.

Blood Cells Mol Dis. 2012 Aug 15;49(2):83-4. doi: 10.1016/j.bcmd.2012.05.006. No abstract available.

PMID:
22658796
18.

Application of MLPA assay to characterize unsolved α-globin gene rearrangements.

Colosimo A, Gatta V, Guida V, Leodori E, Foglietta E, Rinaldi S, Cappabianca MP, Amato A, Stuppia L, Dallapiccola B.

Blood Cells Mol Dis. 2011 Feb 15;46(2):139-44. doi: 10.1016/j.bcmd.2010.11.006.

PMID:
21190870
19.

Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma.

Yan TZ, Mo QH, Cai R, Chen X, Zhang CM, Liu YH, Chen YJ, Zhou WJ, Xiong F, Xu XM.

PLoS One. 2011;6(9):e24779. doi: 10.1371/journal.pone.0024779.

20.

A rare Hb H disease due to the - -(SEA) and 16.6 kb α-thalassemia-2 deletions.

Sroymora S, Jindadamrongwech S, Butthep P, Chuncharunee S.

Hemoglobin. 2012;36(2):200-4. doi: 10.3109/03630269.2012.655355.

PMID:
22376301

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