Similar articles

• Beta-globin-gene haplotypes, mitochondrial DNA, the Y-chromosome: their impact on the genetic epidemiology of the major structural hemoglobinopathies.

  Nagel RL. Nagel RL. Cell Mol Biol (Noisy-le-grand). 2004 Feb;50(1):5-21. Cell Mol Biol (Noisy-le-grand). 2004. PMID: 15040423 Review.
• [Gene diagnosis of hemoglobinopathies--the determination of breakpoints for a large deletion].

  Hattori Y, Yamashiro Y. Hattori Y, et al. Rinsho Byori. 2003 Jun;51(6):550-5. Rinsho Byori. 2003. PMID: 12884742 Review. Japanese.
• Carrier screening and prenatal diagnosis of hemoglobinopathies. A study of indigenous and immigrant couples in northern Greece, over the last 5 years.

  Theodoridou S, Alemayehou M, Prappas N, Karakasidou O, Aletra V, Plata E, Tsaftaridis P, Karababa P, Boussiou M, Sinopoulou K, Hatzi A, Voskaridou E, Loutradi A, Manitsa A. Theodoridou S, et al. Hemoglobin. 2008;32(5):434-9. doi: 10.1080/03630260802341745. Hemoglobin. 2008. PMID: 18932067
• Beta-globin-like gene cluster haplotypes in hemoglobinopathies.

  Muralitharan S, Krishnamoorthy R, Nagel RL. Muralitharan S, et al. Methods Mol Med. 2003;82:195-211. doi: 10.1385/1-59259-373-9:195. Methods Mol Med. 2003. PMID: 12669645 No abstract available.
• Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.

  Kalamaras A, Chassanidis C, Samara M, Papadakis MN, Vagena A, Aleporou-Marinou V, Patrinos GP, Kollia P. Kalamaras A, et al. Am J Hematol. 2008 Sep;83(9):760. doi: 10.1002/ajh.21243. Am J Hematol. 2008. PMID: 18615450 No abstract available.