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Items: 1 to 20 of 83

1.

Annotation error of a common β°-thalassemia mutation (619 bp-deletion) has implications for molecular diagnosis.

Pritchard CC, Tait JF, Buller-Burckle AM, Mikula M.

Am J Hematol. 2010 Dec;85(12):978. doi: 10.1002/ajh.21875. No abstract available.

2.

Genotype-phenotype correlations in beta-thalassemias.

Cao A, Galanello R, Rosatelli MC.

Blood Rev. 1994 Mar;8(1):1-12. Review.

PMID:
8205005
3.
4.

Detection of a rare mutation in an Iranian family: codons 37/38/39 (7 bp deletion).

Zadeh-Vakili A, Eshghi P.

Hemoglobin. 2009;33(6):523-7. doi: 10.3109/03630260903343897.

PMID:
19958201
5.
6.

Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.

Huang G, Jiang WL, Rong KB, Li YX, Luo XL, Meng JX, Yu XY.

Hemoglobin. 2010 Jan;34(2):179-83. doi: 10.3109/03630261003670226.

PMID:
20353356
7.

Molecular basis of beta thalassemia in the south of Thailand.

Laosombat V, Fucharoen SP, Panich V, Fucharoen G, Wongchanchailert M, Sriroongrueng W, Nopparatana C, Kenpitak K, Maipang M, Fukumaki Y.

Am J Hematol. 1992 Nov;41(3):194-8.

PMID:
1415194
8.

Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis.

Waye JS, Patterson M, Walker L, Eng B, Nakamura LM, Lafferty JD, Yong SL, Wu JK, Chui DH.

Am J Hematol. 2003 Nov;74(3):179-81. Erratum in: Am J Hematol. 2004 May;76(1):99. Yong, Sui-Li [corrected to Yong, Siu-Li].

9.

Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemias.

Ghanem N, Vidaud M, Plassa F, Martin J, Goossens M.

Mol Cell Probes. 1993 Apr;7(2):167-8.

PMID:
8321255
10.

Heteroduplex formation: a potential source of genotyping error from PCR products.

Hatcher SL, Lambert QT, Teplitz RL, Carlson JR.

Prenat Diagn. 1993 Mar;13(3):171-7.

PMID:
8506218
11.

A novel deletion in a Turkish beta-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp).

Ozçelik H, Başak AN, Tüzmen S, Kirdar B, Akar N.

Hemoglobin. 1993 Aug;17(4):387-91. No abstract available.

PMID:
8226099
12.

Thalassemia syndromes in Saudi Arabia. Meta-analysis of local studies.

Al-Awamy BH.

Saudi Med J. 2000 Jan;21(1):8-17.

PMID:
11533744
13.

Mutation at -30 (T-->C) of the delta-globin gene in a Taiwanese beta-thalassemia carrier.

Huang CH, Ko TM, Chiang YL, Lin CS.

Hemoglobin. 2003 Aug;27(3):205-9. No abstract available.

PMID:
12908807
14.

[Thalassemia].

Hattori Y.

Rinsho Byori. 1995 Aug;43(8):776-80. Review. Japanese.

PMID:
7474435
15.

Distribution of beta-thalassemia mutations in the Indian population referred to a diagnostic center.

Vaz FE, Thakur CB, Banerjee MK, Gangal SG.

Hemoglobin. 2000 Aug;24(3):181-94.

PMID:
10975438
16.

Carrier screening and prenatal diagnosis of beta-thalassemia.

Maheshwari M, Arora S, Kabra M, Menon PS.

Indian Pediatr. 1999 Nov;36(11):1119-25. Review. No abstract available.

PMID:
10745333
17.

Molecular characterization of deletional forms of beta-thalassemia in Taiwan.

Peng CT, Liu SC, Chiou SS, Kuo PL, Shih MC, Chang JY, Chang JG.

Ann Hematol. 2003 Jan;82(1):33-6. Epub 2002 Nov 29.

PMID:
12574962
18.

Prenatal diagnosis of beta-thalassemia major by high-performance liquid chromatography analysis of hemoglobins in fetal blood samples.

Sanguansermsri T, Thanarattanakorn P, Steger HF, Tongsong T, Chanprapaph P, Wanpirak C, Siriwatanapa P, Sirichotiyakul S, Flatz G.

Hemoglobin. 2001 Feb;25(1):19-27.

PMID:
11300346
19.

High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemia.

Patterson M, Walker L, Eng B, Waye JS.

Hemoglobin. 2005;29(4):293-5.

PMID:
16370492

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