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Hematological features and molecular lesions of hemoglobin gene disorders in Taiwanese patients. [JOURNAL ARTICLE]
Int J Lab Hematol 2008 Aug 14.
Abstract | Full Citation | Find Related Articles | | Sirichotiyakul S, Piyamongkol W, Tongprasert F, et al.
Transabdominal chorionic villus sampling: experience at Maharaj Nakorn Chiang Mai Hospital. [Journal Article]
J Med Assoc Thai 2008 Jun; 91(6):813-7.
Abstract | Full Citation | | Pornprasert S, Kaewbundit A, Phusua A, et al.
Comparison of real-time PCR SYBR Green1 with HRM analysis and TaqMan MGB probes for detection of alpha-thalassemia-1 SEA type on dried blood spots. [JOURNAL ARTICLE]
Eur J Haematol 2008 Aug 8.
Full Citation | Find Related Articles | | Passarello C, Giambona A, Prossomariti L, et al.
Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha(2) 130 Ala-->Pro and Hb Caserta alpha(2) 26 Ala-->Thr) in a single HBA2 gene. [JOURNAL ARTICLE]
Br J Haematol 2008 Aug 4.
Abstract | Full Citation | Find Related Articles | | Juncà J, Mañú-Pereira M, Radó-Trilla N, et al.
Cell counter-based parameters and formulas in detection of beta-thalassemia trait. [Comment, Letter]
Am J Clin Pathol 2008 Jul; 130(1):147-8; author reply 148.
Full Citation | Find Related Articles | | Denic S, Nagelkerke N, Agarwal MM
Consanguineous marriages and endemic malaria: can inbreeding increase population fitness? [JOURNAL ARTICLE]
Malar J 2008 Aug 2; 7(1):150.
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Two new alpha-thalassemia point mutations that are undetectable by biochemical techniques. [Journal Article]
Hemoglobin 2008; 32(4):411-7.
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Analysis of real-time SYBR-polymerase chain reaction cycle threshold for diagnosis of the alpha-thalassemia-1 Southeast Asian type deletion: application to carrier screening and prenatal diagnosis of Hb Bart's hydrops fetalis. [Journal Article, Research Support, Non-U.S. Gov't]
Hemoglobin 2008; 32(4):393-402.
Abstract | Full Citation | Find Related Articles | | Douna V, Papassotiriou I, Metaxotou-Mavrommati A, et al.
Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutations. [Journal Article, Research Support, Non-U.S. Gov't]
Hemoglobin 2008; 32(4):379-85.
Abstract | Full Citation | Find Related Articles | | Douna V, Liapi D, Kampourakis D, et al.
First observation of Hb Taybe [Codons 38/39 (-Acc) Thr-->0 (alpha1)] in Greece: clinical and hematological findings in patients with co-inherited alpha+-thalassemia mutations. [Journal Article, Research Support, Non-U.S. Gov't]
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Abstract | Full Citation | Find Related Articles |   |
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