A novel frameshift mutation [FSC 47 (+A)] causing... [Hemoglobin. 1990] - PubMed

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Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient. [Hemoglobin. 1989]
Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient.
Kollia P, Gonzalez-Redondo JM, Stoming TA, Loukopoulos D, Politis C, Huisman TH. Hemoglobin. 1989; 13(6):597-604.
A possible example of gene conversion with a common beta-thalassemia mutation and Chi sequence present in the beta-globin gene. [Hum Genet. 1992]
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Matsuno Y, Yamashiro Y, Yamamoto K, Hattori Y, Yamamoto K, Ohba Y, Miyaji T. Hum Genet. 1992 Jan; 88(3):357-8.
A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient. [Hemoglobin. 1992]
A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.
Başak AN, Ozer A, Ozçelik H, Kirdar B, Gürgey A. Hemoglobin. 1992; 16(4):309-12.
Review Gene defects in beta-thalassemia and their prenatal diagnosis. [Ann N Y Acad Sci. 1990]
Review Gene defects in beta-thalassemia and their prenatal diagnosis.
Kazazian HH Jr, Dowling CE, Boehm CD, Warren TC, Economou EP, Katz J, Antonarakis SE. Ann N Y Acad Sci. 1990; 612:1-14.
Review The alpha-thalassemias. [Ann N Y Acad Sci. 1990]
Review The alpha-thalassemias.
Higgs DR, Wood WG, Jarman AP, Vickers MA, Wilkie AO, Lamb J, Vyas P, Bennett JP. Ann N Y Acad Sci. 1990; 612:15-22.

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Cited by 1 PubMed Central article

Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis. [J Med Genet. 1992]
Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis.
Losekoot M, van Heeren H, Schipper JJ, Giordano PC, Bernini LF, Fodde R. J Med Genet. 1992 Aug; 29(8):574-7.

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A novel frameshift mutation [FSC 47 (+A)] causing beta-thalassemia in a Surinam ...
A novel frameshift mutation [FSC 47 (+A)] causing beta-thalassemia in a Surinam patient.
Hemoglobin. 1990 ;14(4):467-70.

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