Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 419

1.

Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion.

Basran RK, Reiss UM, Luo HY, Ware RE, Chui DH.

Pediatr Blood Cancer. 2008 Feb;50(2):363-6.

PMID:
16732578
2.

A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.

Chen XW, Mo QH, Li Q, Zeng R, Xu XM.

Ann Hematol. 2007 Sep;86(9):653-7. Epub 2007 May 22.

PMID:
17516066
3.

Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.

Vrettou C, Kanavakis E, Traeger-Synodinos J, Metaxotou-Mavrommati A, Basiakos I, Maragoudaki E, Stamoulakatou A, Papassotiriou I, Kattamis C.

Hemoglobin. 2000 Aug;24(3):203-20.

PMID:
10975440
4.

Mutational spectrum of delta-globin gene in the Portuguese population.

Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.

Eur J Haematol. 2007 Nov;79(5):422-8. Epub 2007 Oct 4.

PMID:
17916081
5.

Dominantly Inherited beta-Thalassemia.

Efremov GD.

Hemoglobin. 2007;31(2):193-207.

PMID:
17486503
6.

Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.

Lemsaddek W, Picanço I, Seuanes F, Mahmal L, Benchekroun S, Khattab M, Nogueira P, Osório-Almeida L.

Am J Hematol. 2003 Jul;73(3):161-8.

7.

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
8.

A novel 105 basepair deletion causing beta(0)-thalassemia in members of a Thai family.

Nopparatana C, Saechan V, Nopparatana C, Pornpatkul M, Panich V, Fukumaki Y.

Am J Hematol. 1999 May;61(1):1-4.

9.

Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients.

Camaschella C, Mazza U, Roetto A, Gottardi E, Parziale A, Travi M, Fattore S, Bacchiega D, Fiorelli G, Cappellini MD.

Am J Hematol. 1995 Feb;48(2):82-7.

PMID:
7847345
10.
11.

Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.

Maragoudaki E, Kanavakis E, Traeger-Synodinos J, Vrettou C, Tzetis M, Metaxotou-Mavrommati A, Kattamis C.

Br J Haematol. 1999 Dec;107(4):699-706.

PMID:
10606872
14.

Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India.

Garewal G, Das R, Ahluwalia J, Marwaha RK, Varma S.

Am J Hematol. 2005 Aug;79(4):252-6.

16.

First Spanish case of thalassemia major due to a compound heterozygosity for the IVS-II-848 (C --> A) and codon 39 (C --> T) mutations of the beta-globin gene.

Ropero P, Villegas A, Muñoz J, Briceño O, Mora A, Salvador M, Polo M, González FA.

Hemoglobin. 2006;30(1):15-21.

PMID:
16540410
17.
18.

Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.

Ragusa A, Amata S, Lombardo T, Castiglia L, Maier-Redelsperger M, Labie D, Bernini L.

Haematologica. 2003 Oct;88(10):1099-105.

19.

[A rare transcription mutation (-90 C-->T) in a Chinese family with beta-thalassemia].

Li WJ, Lao XW, Jai SQ, Liang FA, Mo QH, Ma JY, Xu XM.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Dec;20(6):468-70. Chinese.

PMID:
14669211
20.

[Molecular analysis of beta-thalassemia intermedia in Guangdong Province].

Zhang L, Ou XB, Yu YP.

Zhongguo Dang Dai Er Ke Za Zhi. 2007 Aug;9(4):358-60. Chinese.

PMID:
17706040

Supplemental Content

Support Center